Phospholipid:diacylglycerol acyltransferases

ABSTRACT

This invention relates to an isolated nucleic acid fragment encoding an acyltransferase, more specifically a phospholipid:diacylglycerol acyltransferase. The invention also relates to the construction of a recombinant DNA construct encoding all or a portion of the phospholipid:diacylglycerol acyltransferase, in sense or antisense orientation, wherein expression of the recombinant DNA construct results in production of altered levels of the phospholipid:diacylglycerol acyltransferase in a transformed host cell.

FIELD OF THE INVENTION

[0001] The field of invention relates to plant molecular biology, and more specifically, to nucleic acid fragments encoding phospholipid:diacylglycerol acyltransferases in plants and seeds.

BACKGROUND OF INVENTION

[0002] In eukaryotic cells triacylglycerols are quantitatively the most important storage form of energy. The main pathway for synthesis of triacylglycerol is believed to involve three sequential acyl-transfers from acyl-CoA to the glycerol backbone. Acyl-CoA:diacylglycerol acyltransferase (DAGAT, EC 2.3.1.20) uses fatty acyl-CoA (acyl donor) and 1,2-diacylglycerol (acyl acceptor) as substrates to catalyze the third and only committed step in triacylglycerol synthesis. DAGAT plays a fundamental role in the metabolism of cellular glycerolipids.

[0003] Until recently, it was believed that only DAGAT could carry out the final step in triacylglycerol biosynthesis. However, it has now been demonstrated that microsomal preparation of developing seeds from several plants (sunflower, Helianthus annus; castor bean, Ricinus communis; hawk's beard, Crepis palaestina) as well as microsomal preparations from yeast (Saccharomyces cerevisiae) catalyze triacylglycerol formation via the enzyme phospholipid:diacylglycerol acyltransferase (PDAT, EC 2.3.1.158, Registry Number 288587-47-3) (WO 2000060095; Dahlqvist et al., Proc. Natl. Acad. Sci. USA 97(12):6487-6492 (2000)). This enzyme differs from DAGAT by synthesising triacylglycerol using an acyl-CoA-independent mechanism. The specificity of the enzyme for the acyl group in the phospholipid varies with species, e.g., the enzyme from castor bean preferentially incorporates vernoloyl (12,13-epoxyoctadec-9-enoyl) groups into triacylglycerol, whereas that from the hawk's beard incorporates both ricinoleoyl (12-hydroxyoctadec-9-enoyl) and vernoloyl groups. The enzyme from the yeast Saccharomyces cerevisiae specifically transfers acyl groups from the sn-2 position of the phospholipid to diacylglycerol, thus forming an sn-1-lysophospholipid. It has also been shown that PDAT activity is present in vegetative tissues of Arabidopsis thaliana (Banaś et al., Biochem. Soc. Trans. 28:703-703 (2000)). Furthermore, the substrate specificity of PDAT varies between species and depends on the head group of the acyl donor, the acyl group transferred and the acyl chains of the acyl acceptor (1,2-diacylglycerol).

SUMMARY OF INVENTION

[0004] The present invention concerns isolated polynucleotides comprising a nucleotide sequence encoding a polypeptide having phospholipid:diacylglycerol acyltransferase activity, wherein the amino acid sequence of the polypeptide and the amino acid sequence of SEQ ID NO:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 32, 34 or 36 have at least 80%, 85%, 90% or 95% sequence identity, based on the Clustal V method of alignment. The present invention also relates to isolated polynucleotides comprising the complement of the nucleotide sequence. More specifically, the present invention includes isolated polynucleotides encoding the polypeptide sequence of SEQ ID NO:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 32, 34 or 36 or nucleotide sequences comprising the nucleotide sequence of SEQ ID NO:1, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 27, 31, 33 or 35.

[0005] In a first embodiment, the present invention includes an isolated polynucleotide comprising: (a) a nucleotide sequence encoding a polypeptide having phospholipid:diacylglycerol acyltransferase activity, wherein the polypeptide has an amino acid sequence of at least 80%, 85%, 90%, or 95% sequence identity, based on the Clustal V method of alignment, when compared to one of SEQ ID NO:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 32, 34 or 36, or (b) a complement of the nucleotide sequence, wherein the complement and the nucleotide sequence consist of the same number of nucleotides and are 100% complementary. The polypeptide preferably comprises the amino acid sequence of SEQ ID NO:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 32, 34 or 36. The nucleotide sequence preferably comprises the nucleotide sequence of SEQ ID NO:1, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 27, 31, 33 or 35.

[0006] In a second embodiment, the present invention includes a recombinant DNA construct comprising any of the isolated polynucleotides of the present invention operably linked to at least one regulatory sequence, and a cell, a plant, and a seed comprising the recombinant DNA construct.

[0007] In a third embodiment, the present invention includes a vector comprising any of the isolated polynucleotides of the present invention.

[0008] In a fourth embodiment, the present invention includes a method for transforming a cell comprising transforming a cell with any of the isolated polynucleotides of the present invention. The cell transformed by this method is also included. Advantageously, the cell is eukaryotic, e.g., a yeast or plant cell, or prokaryotic, e.g., a bacterium.

[0009] In a fifth embodiment, the present invention includes a method for producing a transgenic plant comprising transforming a plant cell with any of the isolated polynucleotides of the present invention and regenerating a plant from the transformed plant cell, a transgenic plant produced by this method, and seed obtained from this transgenic plant.

[0010] In a sixth embodiment, the present invention includes an isolated polypeptide having phospholipid:diacylglycerol acyltransferase activity, wherein the polypeptide has an amino acid sequence of at least 80%, 85%, 90%, or 95% identity, based on the Clustal V method of alignment, when compared to one of SEQ ID NO:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 32, 34 or 36. The polypeptide preferably comprises one of SEQ ID NO:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 32, 34 or 36.

[0011] In a seventh embodiment, the present invention includes a method for isolating a polypeptide having phospholipid:diacylglycerol acyltransferase activity comprising isolating the polypeptide from a cell or culture medium of the cell, wherein the cell comprises a recombinant DNA construct comprising a polynucleotide of the invention operably linked to at least one regulatory sequence.

[0012] In an eighth embodiment, this invention includes a method for selecting a transformed cell comprising: (a) transforming a host cell with the recombinant DNA construct or an expression cassette of the present invention; and (b) growing the transformed host cell, preferably a plant cell, under conditions that allow expression of the phospholipid:diacylglycerol acyltransferase polynucleotide in an amount sufficient to complement a null mutant in order to provide a positive selection means.

[0013] In a ninth embodiment, this invention includes a method of altering the level of expression of a phospholipid:diacylglycerol acyltransferase protein in a host cell comprising: (a) transforming a host cell with a recombinant DNA construct of the present invention; and (b) growing the transformed host cell under conditions that are suitable for expression of the recombinant DNA construct wherein expression of the recombinant DNA construct results in production of altered levels of the phospholipid:diacylglycerol acyltransferase protein in the transformed host cell.

BRIEF DESCRIPTION OF THE DRAWINGS AND SEQUENCE LISTING

[0014]FIGS. 1A, 1B, 1C, 1D, 1E and 1F show a comparison of the amino acid sequences of the phospholipid:diacylglycerol acyltransferase (PDAT) 2 encoded by the following: (a) nucleotide sequence derived from guar clone lds3c.pk001.j8:fis (SEQ ID NO:16), (b) nucleotide sequence derived from guayule clone epb3c.pk008.j11:fis (SEQ ID NO:18), (c) nucleotide sequence of a contig assembled from corn clone cds2f.pk002.k4:fis (SEQ ID NO:20), (d) nucleotide sequence derived from rice clone rlr6.pk0092.c4:fis (SEQ ID NO:22), (e) nucleotide sequence derived from soybean clone sdp2c.pk034.e7:fis (SEQ ID NO:24), (f) nucleotide sequence derived from sunflower clone hlp1c.pk004.i1:fis (SEQ ID NO:26), (g) nucleotide sequence of a contig assembled from nucleotide sequences derived from wheat clones wip1c.pk005.b24:fis and wlm96.pk0006.f11 (SEQ ID NO:28), (h) nucleotide sequence derived from soybean clone sgs4c.pk006.b20:fis (SEQ ID NO:36) and (i) nucleotide sequence from Arabidopsis thaliana (NCBI General Identification (GI) No. 15240676; SEQ ID NO:30). Dashes are used by the program to maximize alignment of the sequences.

[0015]FIGS. 2A, 2B, 2C, 2D and 2E show a comparison of the amino acid sequences of the phospholipid:diacylglycerol acyltransferase (PDAT) 1 encoded by the following: (a) nucleotide sequence derived from balsam pear clone fds.pk0003.b4:fis (SEQ ID NO:2), (b) nucleotide sequence derived from pot marigold clone ecs1c.pk009.j18:fis (SEQ ID NO:4), (c) nucleotide sequence derived from eucalyptus clone eef1c.pk006.c14:fis (SEQ ID NO:6), (d) nucleotide sequence derived from grape clone vmb1na.pk016.c2:fis (SEQ ID NO:8), (e) nucleotide sequence derived from rice clone rsr9n.pk002.f3:fis (SEQ ID NO:10), (f) nucleotide sequence derived from vernonia clone vs1n.pk016.n3:fis (SEQ ID NO:12), (g) nucleotide sequence derived from wheat clone wpa1c.pk009.g15 (SEQ ID NO:14, (h) nucleotide sequence derived from guar clone lds3c.pk008.f17:fis (SEQ ID NO: 32), (i) nucleotide sequence derived from wheat clone wpa1c.pk009.g15:fis (SEQ ID NO:34) and (j) nucleotide sequence from Arabidopsis thaliana (NCBI General Identification (GI) No. 7452457; SEQ ID NO:29). Dashes are used by the program to maximize alignment of the sequences.

[0016] Table 1 lists the polypeptides that are described herein, the designation of the cDNA clones that comprise the nucleic acid fragments encoding polypeptides representing all or a substantial portion of these polypeptides, and the corresponding identifier (SEQ ID NO:) as used in the attached Sequence Listing. The sequence descriptions and Sequence Listing attached hereto comply with the rules governing nucleotide and/or amino acid sequence disclosures in patent applications as set forth in 37 C.F.R. §1.821-1.825. TABLE 1 Phospholipid:diacylglycerol Acyltransferases SEQ ID NO: Protein Clone Designation (Nucleotide) (Amino Acid) Balsam Pear Polypeptide fds.pk0003.b4:fis 1 2 Similar to Arabidopsis thaliana PDAT 1 Calendula Polypeptide Similar Ecs1c.pk009.j18:fis 3 4 to Arabidopsis thaliana PDAT 1 Eucalyptus Polypeptide Similar Eef1c.pk006.c14:fis 5 6 to Arabidopsis thaliana PDAT 1 Grape Polypeptide Similar to Vmb1na.pk016.c2:fis 7 8 Arabidopsis thaliana PDAT 1 Rice Polypeptide Similar to rsr9n.pk002.f3:fis 9 10 Arabidopsis thaliana PDAT 1 Vernonia Polypeptide Similar to vs1n.pk016.n3:fis 11 12 Arabidopsis thaliana PDAT 1 Wheat Polypeptide Similar to Wpa1c.pk009.g15 13 14 Arabidopsis thaliana PDAT 1 Guar Polypeptide Similar to Lds3c.pk008.f17:fis 31 32 Arabidopsis thaliana PDAT 1 Wheat Polypeptide Similar to Wpa1c.pk009.g15:fis 33 34 Arabidopsis thaliana PDAT 1 Guar Polypeptide Similar to Lds3c.pk001.j8:fis 15 16 Arabidopsis thaliana PDAT 2 Guayule Polypeptide Similar to Epb3c.pk008.j11:fis 17 18 Arabidopsis thaliana PDAT 2 Corn Polypeptide Similar to Contig of: 19 20 Arabidopsis thaliana PDAT 2 Cds2f.pk002.k4:fis Rice Polypeptide Similar to rlr6.pk0092.c4:fis 21 22 Arabidopsis thaliana PDAT 2 Soybean Polypeptide Similar to Sdp2c.pk034.e7:fis 23 24 Arabidopsis thaliana PDAT 2 Sunflower Polypeptide Similar Hlp1c.pk004.i1:fis 25 26 to Arabidopsis thaliana PDAT 2 Wheat Polypeptide Similar to Contig of: 27 28 Arabidopsis thaliana PDAT 2 Wip1c.pk005.b24:fis Wlm96.pk0006.f11 Soybean Polypeptide Similar to Sgs4c.pk006.b20:fis 35 36 Arabidopsis thaliana PDAT 2

[0017] SEQ ID NO:29 is the amino acid sequence of Arabidopsis thaliana (NCBI General Identification (GI) No. 7452457). NCBI General Identifier No. 7452457 is 100% identical to NCBI General Identifier No. 15235214 and NCBI Accession No. CAA19703. Arabidopsis thaliana CAA19703 can be found in FIG. 5 of Dahlqvist et al., Proc. Natl. Acad. Sci. USA 97(12):6487-6492 (2000).

[0018] SEQ ID NO:30 is the amino acid sequence of Arabidopsis thaliana (NCBI General Identification (GI) No. 15240676). NCBI General Identifier No. 15240676 is 100% identical to NCBI General Identifier No. 9758029 and NCBI Accession No. AB006704. Arabidopsis thaliana AB006704 can be found in FIG. 5 of Dahlqvist et al., Proc. Natl. Acad. Sci. USA 97(12):6487-6492 (2000).

[0019] The Sequence Listing contains the one letter code for nucleotide sequence characters and the three letter codes for amino acids as defined in conformity with the IUPAC-IUBMB standards described in Nucleic Acids Res. 13:3021-3030 (1985) and in the Biochemical J. 219 (No. 2):345-373 (1984) which are herein incorporated by reference. The symbols and format used for nucleotide and amino acid sequence data comply with the rules set forth in 37 C.F.R. §1.822.

DETAILED DESCRIPTION OF THE INVENTION

[0020] The disclosure of each reference set forth herein is incorporated herein by reference in its entirety.

[0021] In the context of this disclosure, a number of terms shall be utilized. The terms “polynucleotide”, “polynucleotide sequence”, “nucleic acid sequence”, and “nucleic acid fragment”/“isolated nucleic acid fragment” are used interchangeably herein. These terms encompass nucleotide sequences and the like. A polynucleotide may be a polymer of RNA or DNA that is single- or double-stranded, that optionally contains synthetic, non-natural or altered nucleotide bases. A polynucleotide in the form of a polymer of DNA may be comprised of one or more segments of cDNA, genomic DNA, synthetic DNA, or mixtures thereof. An isolated polynucleotide of the present invention may include at least 30 contiguous nucleotides, preferably at least 40 contiguous nucleotides, most preferably at least 60 contiguous nucleotides derived from SEQ ID NO:1, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 27, 31, 33 or 35, or the complement of such sequences.

[0022] The term “isolated” refers to materials, such as nucleic acid molecules and/or proteins, which are substantially free or otherwise removed from components that normally accompany or interact with the materials in a naturally occurring environment. Isolated polynucleotides may be purified from a host cell in which they naturally occur. Conventional nucleic acid purification methods known to skilled artisans may be used to obtain isolated polynucleotides. The term also embraces recombinant polynucleotides and chemically synthesized polynucleotides.

[0023] The term “recombinant” means, for example, that a nucleic acid sequence is made by an artificial combination of two otherwise separated segments of sequence, e.g., by chemical synthesis or by the manipulation of isolated nucleic acids by genetic engineering techniques. A “recombinant DNA construct” comprises any of the isolated polynucleotides of the present invention operably linked to at least one regulatory sequence.

[0024] As used herein, “contig” refers to a nucleotide sequence that is assembled from two or more constituent nucleotide sequences that share common or overlapping regions of sequence homology. For example, the nucleotide sequences of two or more nucleic acid fragments can be compared and aligned in order to identify common or overlapping sequences. Where common or overlapping sequences exist between two or more nucleic acid fragments, the sequences (and thus their corresponding nucleic acid fragments) can be assembled into a single contiguous nucleotide sequence.

[0025] As used herein, “substantially similar” refers to nucleic acid fragments wherein changes in one or more nucleotide bases results in substitution of one or more amino acids, but do not affect the functional properties of the polypeptide encoded by the nucleotide sequence. “Substantially similar” also refers to nucleic acid fragments wherein changes in one or more nucleotide bases does not affect the ability of the nucleic acid fragment to mediate alteration of gene expression by gene silencing through for example antisense or co-suppression technology. “Substantially similar” also refers to modifications of the nucleic acid fragments of the instant invention such as deletion or insertion of one or more nucleotides that do not substantially affect the functional properties of the resulting transcript vis-á-vis the ability to mediate gene silencing or alteration of the functional properties of the resulting protein molecule. It is therefore understood that the invention encompasses more than the specific exemplary nucleotide or amino acid sequences and includes functional equivalents thereof. The terms “substantially similar” and “corresponding substantially” are used interchangeably herein.

[0026] Substantially similar nucleic acid fragments may be selected by screening nucleic acid fragments representing subfragments or modifications of the nucleic acid fragments of the instant invention, wherein one or more nucleotides are substituted, deleted and/or inserted, for their ability to affect the level of the polypeptide encoded by the unmodified nucleic acid fragment in a plant or plant cell. For example, a substantially similar nucleic acid fragment representing at least 30 contiguous nucleotides, preferably at least 40 contiguous nucleotides, most preferably at least 60 contiguous nucleotides derived from the instant nucleic acid fragment can be constructed and introduced into a plant or plant cell. The level of the polypeptide encoded by the unmodified nucleic acid fragment present in a plant or plant cell exposed to the substantially similar nucleic fragment can then be compared to the level of the polypeptide in a plant or plant cell that is not exposed to the substantially similar nucleic acid fragment.

[0027] For example, it is well known in the art that antisense suppression and co-suppression of gene expression may be accomplished using nucleic acid fragments representing less than the entire coding region of a gene, and by using nucleic acid fragments that do not share 100% sequence identity with the gene to be suppressed. Moreover, alterations in a nucleic acid fragment which result in the production of a chemically equivalent amino acid at a given site, but do not effect the functional properties of the encoded polypeptide, are well known in the art. Thus, a codon for the amino acid alanine, a hydrophobic amino acid, may be substituted by a codon encoding another less hydrophobic residue, such as glycine, or a more hydrophobic residue, such as valine, leucine, or isoleucine. Similarly, changes which result in substitution of one negatively charged residue for another, such as aspartic acid for glutamic acid, or one positively charged residue for another, such as lysine for arginine, can also be expected to produce a functionally equivalent product. Nucleotide changes which result in alteration of the N-terminal and C-terminal portions of the polypeptide molecule would also not be expected to alter the activity of the polypeptide. Each of the proposed modifications is well within the routine skill in the art, as is determination of retention of biological activity of the encoded products. Consequently, an isolated polynucleotide comprising a nucleotide sequence of at least 30 (preferably at least 40, most preferably at least 60) contiguous nucleotides derived from a nucleotide sequence selected from the group consisting of SEQ ID NO:1, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 27, 31, 33 or 35, and the complement of such nucleotide sequences may be used to affect the expression and/or function of a phospholipid:diacylglycerol acyltransferases (PDAT 1 or PDAT 2) in a host cell. A method of using an isolated polynucleotide to affect the level of expression of a polypeptide in a host cell (eukaryotic, such as plant or yeast, prokaryotic such as bacterial) may comprise the steps of: constructing an isolated polynucleotide of the present invention or an isolated recombinant DNA construct of the present invention; introducing the isolated polynucleotide or isolated recombinant DNA construct into a host cell; measuring the level of a polypeptide or enzyme activity in the host cell containing the isolated polynucleotide; and comparing the level of a polypeptide or enzyme activity in the host cell containing the isolated polynucleotide with the level of a polypeptide or enzyme activity in a host cell that does not contain the isolated polynucleotide.

[0028] Moreover, substantially similar nucleic acid fragments may also be characterized by their ability to hybridize. Estimates of such homology are provided by either DNA-DNA or DNA-RNA hybridization under conditions of stringency as is well understood by those skilled in the art (Hames and Higgins, Eds. (1985) Nucleic Acid Hybridisation, IRL Press, Oxford, U.K.). Stringency conditions can be adjusted to screen for moderately similar fragments, such as homologous sequences from distantly related organisms, to highly similar fragments, such as genes that duplicate functional enzymes from closely related organisms. Post-hybridization washes determine stringency conditions. One set of preferred conditions uses a series of washes starting with 6×SSC, 0.5% SDS at room temperature for 15 min, then repeated with 2×SSC, 0.5% SDS at 45° C. for 30 min, and then repeated twice with 0.2×SSC, 0.5% SDS at 50° C. for 30 min. A more preferred set of stringent conditions uses higher temperatures in which the washes are identical to those above except for the temperature of the final two 30 min washes in 0.2×SSC, 0.5% SDS was increased to 60° C. Another preferred set of highly stringent conditions uses two final washes in 0.1×SSC, 0.1% SDS at 65° C.

[0029] Substantially similar nucleic acid fragments of the instant invention may also be characterized by the percent identity of the amino acid sequences that they encode to the amino acid sequences disclosed herein, as determined by algorithms commonly employed by those skilled in this art. Suitable nucleic acid fragments (isolated polynucleotides of the present invention) encode polypeptides that are at least about 75% identical, preferably at least about 80% identical to the amino acid sequences reported herein. Preferred nucleic acid fragments encode amino acid sequences that are at least about 85% identical to the amino acid sequences reported herein. More preferred nucleic acid fragments encode amino acid sequences that are at least about 90% identical to the amino acid sequences reported herein. Most preferred are nucleic acid fragments that encode amino acid sequences that are at least about 95% identical to the amino acid sequences reported herein. Suitable nucleic acid fragments not only have the above identities but typically encode a polypeptide having at least 50 amino acids, preferably at least 100 amino acids, more preferably at least 150 amino acids, still more preferably at least 200 amino acids, and most preferably at least 250 amino acids. Sequence alignments and percent identity calculations were performed using the Megalign program of the LASERGENE bioinformatics computing suite (DNASTAR Inc., Madison, Wis.). Multiple alignment of the sequences was performed using the Clustal V method of alignment (Higgins and Sharp (1989) CABIOS. 5:151-153) with the default parameters (GAP PENALTY=10, GAP LENGTH PENALTY=10). Default parameters for pairwise alignments using the Clustal V method of alignment were KTUPLE 1, GAP PENALTY=3, WINDOW=5 and DIAGONALS SAVED=5.

[0030] A “substantial portion” of an amino acid or nucleotide sequence comprises an amino acid or a nucleotide sequence that is sufficient to afford putative identification of the protein or gene that the amino acid or nucleotide sequence comprises. Amino acid and nucleotide sequences can be evaluated either manually by one skilled in the art, or by using computer-based sequence comparison and identification tools that employ algorithms such as BLAST (Basic Local Alignment Search Tool; Altschul et al. (1993) J. Mol. Biol. 215:403-410; see also the explanation of the BLAST alogarithm on the world wide web site for the National Center for Biotechnology Information at the National Library of Medicine of the National Institutes of Health). In general, a sequence of ten or more contiguous amino acids or thirty or more contiguous nucleotides is necessary in order to putatively identify a polypeptide or nucleic acid sequence as homologous to a known protein or gene. Moreover, with respect to nucleotide sequences, gene-specific oligonucleotide probes comprising 30 or more contiguous nucleotides may be used in sequence-dependent methods of gene identification (e.g., Southern hybridization) and isolation (e.g., in situ hybridization of bacterial colonies or bacteriophage plaques). In addition, short oligonucleotides of 12 or more nucleotides may be used as amplification primers in PCR in order to obtain a particular nucleic acid fragment comprising the primers. Accordingly, a “substantial portion” of a nucleotide sequence comprises a nucleotide sequence that will afford specific identification and/or isolation of a nucleic acid fragment comprising the sequence. The instant specification teaches amino acid and nucleotide sequences encoding polypeptides that comprise one or more particular plant proteins. The skilled artisan, having the benefit of the sequences as reported herein, may now use all or a substantial portion of the disclosed sequences for purposes known to those skilled in this art. Accordingly, the instant invention comprises the complete sequences as reported in the accompanying Sequence Listing, as well as substantial portions of those sequences as defined above.

[0031] “Codon degeneracy” refers to divergence in the genetic code permitting variation of the nucleotide sequence without effecting the amino acid sequence of an encoded polypeptide. Accordingly, the instant invention relates to any nucleic acid fragment comprising a nucleotide sequence that encodes all or a substantial portion of the amino acid sequences set forth herein. The skilled artisan is well aware of the “codon-bias” exhibited by a specific host cell in usage of nucleotide codons to specify a given amino acid. Therefore, when synthesizing a nucleic acid fragment for improved expression in a host cell, it is desirable to design the nucleic acid fragment such that its frequency of codon usage approaches the frequency of preferred codon usage of the host cell.

[0032] “Synthetic nucleic acid fragments” can be assembled from oligonucleotide building blocks that are chemically synthesized using procedures known to those skilled in the art. These building blocks are ligated and annealed to form larger nucleic acid fragments which may then be enzymatically assembled to construct the entire desired nucleic acid fragment. “Chemically synthesized”, as related to a nucleic acid fragment, means that the component nucleotides were assembled in vitro. Manual chemical synthesis of nucleic acid fragments may be accomplished using well established procedures, or automated chemical synthesis can be performed using one of a number of commercially available machines. Accordingly, the nucleic acid fragments can be tailored for optimal gene expression based on optimization of the nucleotide sequence to reflect the codon bias of the host cell. The skilled artisan appreciates the likelihood of successful gene expression if codon usage is biased towards those codons favored by the host. Determination of preferred codons can be based on a survey of genes derived from the host cell where sequence information is available.

[0033] “Gene” refers to a nucleic acid fragment that expresses a specific protein, including regulatory sequences preceding (5′ non-coding sequences) and following (3′ non-coding sequences) the coding sequence. “Native gene” refers to a gene as found in nature with its own regulatory sequences. “Chimeric gene” refers any gene that is not a native gene, comprising regulatory and coding sequences that are not found together in nature. Accordingly, a chimeric gene may comprise regulatory sequences and coding sequences that are derived from different sources, or regulatory sequences and coding sequences derived from the same source, but arranged in a manner different than that found in nature. “Endogenous gene” refers to a native gene in its natural location in the genome of an organism. A “foreign-gene” refers to a gene not normally found in the host organism, but that is introduced into the host organism by gene transfer. Foreign genes can comprise native genes inserted into a non-native organism, or chimeric genes. A “transgene” is a gene that has been introduced into the genome by a transformation procedure.

[0034] “Coding sequence” refers to a nucleotide sequence that codes for a specific amino acid sequence. “Regulatory sequences” refer to nucleotide sequences located upstream (5′ non-coding sequences), within, or downstream (3′ non-coding sequences) of a coding sequence, and which influence the transcription, RNA processing or stability, or translation of the associated coding sequence. Regulatory sequences may include promoters, translation leader sequences, introns, and polyadenylation recognition sequences.

[0035] “Promoter” refers to a nucleotide sequence capable of controlling the expression of a coding sequence or functional RNA. In general, a coding sequence is located 3′ to a promoter sequence. The promoter sequence consists of proximal and more distal upstream elements, the latter elements often referred to as enhancers. Accordingly, an “enhancer” is a nucleotide sequence which can stimulate promoter activity and may be an innate element of the promoter or a heterologous element inserted to enhance the level or tissue-specificity of a promoter. Promoters may be derived in their entirety from a native gene, or may be composed of different elements derived from different promoters found in nature, or may even comprise synthetic nucleotide segments. It is understood by those skilled in the art that different promoters may direct the expression of a gene in different tissues or cell types, or at different stages of development, or in response to different environmental conditions. Promoters which cause a nucleic acid fragment to be expressed in most cell types at most times are commonly referred to as “constitutive promoters”. New promoters of various types useful in plant cells are constantly being discovered; numerous examples may be found in the compilation by Okamuro and Goldberg (1989) Biochemistry of Plants 15:1-82. It is further recognized that since in most cases the exact boundaries of regulatory sequences have not been completely defined, nucleic acid fragments of different lengths may have identical promoter activity.

[0036] “Translation leader sequence” refers to a nucleotide sequence located between the promoter sequence of a gene and the coding sequence. The translation leader sequence is present in the fully processed mRNA upstream of the translation start sequence. The translation leader sequence may affect processing of the primary transcript to mRNA, mRNA stability or translation efficiency. Examples of translation leader sequences have been described (Turner and Foster (1995) Mol. Biotechnol. 3:225-236).

[0037] “3′ non-coding sequences” refer to nucleotide sequences located downstream of a coding sequence and include polyadenylation recognition sequences and other sequences encoding regulatory signals capable of affecting mRNA processing or gene expression. The polyadenylation signal is usually characterized by affecting the addition of polyadenylic acid tracts to the 3′ end of the mRNA precursor. The use of different 3′ non-coding sequences is exemplified by Ingelbrecht et al. (1989) Plant Cell 1:671-680.

[0038] “RNA transcript” refers to the product resulting from RNA polymerase-catalyzed transcription of a DNA sequence. When the RNA transcript is a perfect complementary copy of the DNA sequence, it is referred to as the primary transcript or it may be a RNA sequence derived from posttranscriptional processing of the primary transcript and is referred to as the mature RNA. “Messenger RNA (mRNA)” refers to the RNA that is without introns and that can be translated into polypeptides by the cell. “cDNA” refers to DNA that is complementary to and derived from an mRNA template. The cDNA can be single-stranded or converted to double stranded form using, for example, the Klenow fragment of DNA polymerase I. “Sense-RNA” refers to an RNA transcript that includes the mRNA and so can be translated into a polypeptide by the cell. “Antisense RNA” refers to an RNA transcript that is complementary to all or part of a target primary transcript or mRNA and that blocks the expression of a target gene (see U.S. Pat. No. 5,107,065, incorporated herein by reference). The complementarity of an antisense RNA may be with any part of the specific nucleotide sequence, i.e., at the 5′ non-coding sequence, 3′ non-coding sequence, introns, or the coding sequence. “Functional RNA” refers to sense RNA, antisense RNA, ribozyme RNA, or other RNA that may not be translated but yet has an effect on cellular processes.

[0039] The term “operably linked” refers to the association of two or more nucleic acid fragments on a single polynucleotide so that the function of one is affected by the other. For example, a promoter is operably linked with a coding sequence when it is capable of affecting the expression of that coding sequence (i.e., that the coding sequence is under the transcriptional control of the promoter). Coding sequences can be operably linked to regulatory sequences in sense or antisense orientation.

[0040] The term “expression”, as used herein, refers to the transcription and stable accumulation of sense (mRNA) or antisense RNA derived from the nucleic acid fragment of the invention. Expression may also refer to translation of mRNA into a polypeptide. “Antisense inhibition” refers to the production of antisense RNA transcripts capable of suppressing the expression of the target protein. “Overexpression” refers to the production of a gene product in transgenic organisms that exceeds levels of production in normal or non-transformed organisms. “Co-suppression” refers to the production of sense RNA transcripts capable of suppressing the expression of identical or substantially similar foreign or endogenous genes (U.S. Pat. No. 5,231,020, incorporated herein by reference).

[0041] A “protein” or “polypeptide” is a chain of amino acids arranged in a specific order determined by the coding sequence in a polynucleotide encoding the polypeptide. Each protein or polypeptide has a unique function.

[0042] “Altered levels” or “altered expression” refers to the production of gene product(s) in transgenic organisms in amounts or proportions that differ from that of normal or non-transformed organisms.

[0043] “Mature protein” or the term “mature” when used in describing a protein refers to a post-translationally processed polypeptide; i.e., one from which any pre-or propeptides present in the primary translation product have been removed. “Precursor protein” or the term “precursor” when used in describing a protein refers to the primary product of translation of mRNA; i.e., with pre- and propeptides still present. Pre- and propeptides may be but are not limited to intracellular localization signals.

[0044] A “chloroplast transit peptide” is an amino acid sequence which is translated in conjunction with a protein and directs the protein to the chloroplast or other plastid types present in the cell in which the protein is made. “Chloroplast transit sequence” refers to a nucleotide sequence that encodes a chloroplast transit peptide. A “signal peptide” is an amino acid sequence which is translated in conjunction with a protein and directs the protein to the secretory system (Chrispeels (1991) Ann. Rev. Plant Phys. Plant Mol. Biol. 42:21-53). If the protein is to be directed to a vacuole, a vacuolar targeting signal (supra) can further be added, or if to the endoplasmic reticulum, an endoplasmic reticulum retention signal (supra) may be added. If the protein is to be directed to the nucleus, any signal peptide present should be removed and instead a nuclear localization signal included (Raikhel (1992) Plant Phys. 100:1627-1632).

[0045] “Transformation” refers to the transfer of a nucleic acid fragment into the genome of a host organism, resulting in genetically stable inheritance. Host organisms containing the transformed nucleic acid fragments are referred to as “transgenic” organisms. Examples of methods of plant transformation include Agrobacterium-mediated transformation (De Blaere et al. (1987) Meth. Enzymol. 143:277) and particle-accelerated or “gene gun” transformation technology (Klein et al. (1987) Nature (London) 327:70-73; U.S. Pat. No. 4,945,050, incorporated herein by reference). Thus, isolated polynucleotides of the present invention can be incorporated into recombinant constructs, typically DNA constructs, capable of introduction into and replication in a host cell. Such a construct can be a vector that includes a replication system and sequences that are capable of transcription and translation of a polypeptide-encoding sequence in a given host cell. A number of vectors suitable for stable transfection of plant cells or for the establishment of transgenic plants have been described in, e.g., Pouwels et al., Cloning Vectors: A Laboratory Manual, 1985, supp. 1987; Weissbach and Weissbach, Methods for Plant Molecular Biology, Academic Press, 1989; and Flevin et al., Plant Molecular Biology Manual, Kluwer Academic Publishers, 1990. Typically, plant expression vectors include, for example, one or more cloned plant genes under the transcriptional control of 5′ and 3′ regulatory sequences and a dominant selectable marker. Such plant expression vectors also can contain a promoter regulatory region (e.g., a regulatory region controlling inducible or constitutive, environmentally- or developmentally-regulated, or cell- or tissue-specific expression), a transcription initiation start site, a ribosome binding site, an RNA processing signal, a transcription termination site, and/or a polyadenylation signal.

[0046] Standard recombinant DNA and molecular cloning techniques used herein are well known in the art and are described more fully in Sambrook et al. Molecular Cloning: A Laboratory Manual; Cold Spring Harbor Laboratory Press: Cold Spring Harbor, 1989 (hereinafter “Maniatis”).

[0047] “PCR” or “polymerase chain reaction” is well known by those skilled in the art as a technique used for the amplification of specific DNA segments (U.S. Pat. Nos. 4,683,195 and 4,800,159).

[0048] The present invention includes an isolated polynucleotide comprising a nucleotide sequence encoding a phospholipid:diacylglycerol acyltransferase polypeptide having at least 80% identity, based on the Clustal V method of alignment, when compared to a polypeptide selected from the group consisting of SEQ ID NO:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 32, 34 or 36.

[0049] This invention also includes the isolated complement of such polynucleotides, wherein the complement and the polynucleotide consist of the same number of nucleotides, and the nucleotide sequences of the complement and the polynucleotide have 100% complementarity.

[0050] Nucleic acid fragments encoding at least a portion of several phospholipid:diacylglycerol acyltransferases have been isolated and identified by comparison of random plant cDNA sequences to public databases containing nucleotide and protein sequences using the BLAST algorithms well known to those skilled in the art. The nucleic acid fragments of the instant invention may be used to isolate cDNAs and genes encoding homologous proteins from the same or other plant species. Isolation of homologous genes using sequence-dependent protocols is well known in the art. Examples of sequence-dependent protocols include, but are not limited to, methods of nucleic acid hybridization, and methods of DNA and RNA amplification as exemplified by various uses of nucleic acid amplification technologies (e.g., polymerase chain reaction, ligase chain reaction).

[0051] For example, genes encoding other phospholipid:diacylglycerol acyltransferases (PDAT 1 or PDAT 2), either as cDNAs or genomic DNAs, could be isolated directly by using all or a portion of the instant nucleic acid fragments as DNA hybridization probes to screen libraries from any desired plant employing methodology well known to those skilled in the art. Specific oligonucleotide probes based upon the instant nucleic acid sequences can be designed and synthesized by methods known in the art (Maniatis). Moreover, an entire sequence can be used directly to synthesize DNA probes by methods known to the skilled artisan such as random primer DNA labeling, nick translation, end-labeling techniques, or RNA probes using available in vitro transcription systems. In addition, specific primers can be designed and used to amplify a part or all of the instant sequences. The resulting amplification products can be labeled directly during amplification reactions or labeled after amplification reactions, and used as probes to isolate full length cDNA or genomic fragments under conditions of appropriate stringency.

[0052] In addition, two short segments of the instant nucleic acid fragments may be used in polymerase chain reaction protocols to amplify longer nucleic acid fragments encoding homologous genes from DNA or RNA. The polymerase chain reaction may also be performed on a library of cloned nucleic acid fragments wherein the sequence of one primer is derived from the instant nucleic acid fragments, and the sequence of the other primer takes advantage of the presence of the polyadenylic acid tracts to the 3′ end of the mRNA precursor encoding plant genes. Alternatively, the second primer sequence may be based upon sequences derived from the cloning vector. For example, the skilled artisan can follow the RACE protocol (Frohman et al. (1988) Proc. Natl. Acad. Sci. USA 85:8998-9002) to generate cDNAs by using PCR to amplify copies of the region between a single point in the transcript and the 3′ or 5′ end. Primers oriented in the 3′ and 5′ directions can be designed from the instant sequences. Using commercially available 3′ RACE or 5′ RACE systems (BRL), specific 3′ or 5′ cDNA fragments can be isolated (Ohara et al. (1989) Proc. Natl. Acad. Sci. USA 86:5673-5677; Loh et al. (1989) Science 243:217-220). Products generated by the 3′ and 5′ RACE procedures can be combined to generate full-length cDNAs (Frohman and Martin (1989) Techniques 1:165). Consequently, a polynucleotide comprising a nucleotide sequence of at least 30 (preferably at least 40, most preferably at least 60) contiguous nucleotides derived from a nucleotide sequence selected from the group consisting of SEQ ID NO:1, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 27, 31, 33 or 35 and the complement of such nucleotide sequences may be used in such methods to obtain a nucleic acid fragment encoding a substantial portion of an amino acid sequence of a polypeptide.

[0053] Availability of the instant nucleotide and deduced amino acid sequences facilitates immunological screening of cDNA expression libraries. Synthetic peptides representing portions of the instant amino acid sequences may be synthesized. These peptides can be used to immunize animals to produce polyclonal or monoclonal antibodies with specificity for peptides or proteins comprising the amino acid sequences. These antibodies can be then be used to screen cDNA expression libraries to isolate full-length cDNA clones of interest (Lerner (1984) Adv. Immunol. 36:1-34; Maniatis).

[0054] In another embodiment, this invention includes viruses and host cells comprising either the recombinant DNA constructs of the invention as described herein or an isolated polynucleotide or recombinant DNA construct of the invention as described herein. Examples of host cells which can be used to practice the invention include, but are not limited to, yeast, bacteria, and plants.

[0055] The nucleic acid fragments of the instant invention may be used to create transgenic plants in which the disclosed polypeptides are present at higher or lower levels than normal or in cell types or developmental stages in which they are not normally found. This would have the effect of altering the level of oil (triacylglycerol) in those cells. The genes of the instant invention may also be used in plant cells to alter the type of oil (triacylglycerol) produced in the cells. PDAT may be a critical enzyme in the metabolism of unusual fatty acids. More specifically, PDAT may be used to accumulate high amounts of uncommon fatty acids from renewable plant resources which have industrial potential. Accordingly, the availability of nucleic acid sequences encoding all or a portion of the enzyme phospholipid:diacylglycerol acyltransferase (PDAT) would facilitate studies to better understand triacylglycerol biosynthesis in plants and provide genetic tools to alter triacylglycerol metabolism.

[0056] Overexpression of the proteins of the instant invention may be accomplished by first constructing a recombinant DNA construct in which the coding region is operably linked to a promoter capable of directing expression of a gene in the desired tissues at the desired stage of development. The recombinant DNA construct may comprise promoter sequences and translation leader sequences derived from the same genes. 3′ Non-coding sequences encoding transcription termination signals may also be provided. The instant recombinant DNA construct may also comprise one or more introns in order to facilitate gene expression.

[0057] Plasmid vectors comprising the instant isolated polynucleotide (or recombinant DNA construct) may be constructed. The choice of plasmid vector is dependent upon the method that will be used to transform host plants. The skilled artisan is well aware of the genetic elements that must be present on the plasmid vector in order to successfully transform, select and propagate host cells containing the recombinant DNA construct. The skilled artisan will also recognize that different independent transformation events will result in different levels and patterns of expression (Jones et al. (1985) EMBO J. 4:2411-2418; De Almeida et al. (1989) Mol. Gen. Genetics 218:78-86), and thus that multiple events must be screened in order to obtain lines displaying the desired expression level and pattern. Such screening may be accomplished by Southern analysis of DNA, Northern analysis of mRNA expression, Western analysis of protein expression, or phenotypic analysis.

[0058] For some applications it may be useful to direct the instant polypeptides to different cellular compartments, or to facilitate its secretion from the cell. It is thus envisioned that the recombinant DNA construct described above may be further supplemented by directing the coding sequence to encode the instant polypeptides with appropriate intracellular targeting sequences such as transit sequences (Keegstra (1989) Cell 56:247-253), signal sequences or sequences encoding endoplasmic reticulum localization (Chrispeels (1991) Ann. Rev. Plant Phys. Plant Mol. Biol. 42:21-53), or nuclear localization signals (Raikhel (1992) Plant Phys. 100:1627-1632) with or without removing targeting sequences that are already present. While the references cited give examples of each of these, the list is not exhaustive and more targeting signals of use may be discovered in the future.

[0059] It may also be desirable to reduce or eliminate expression of genes encoding the instant polypeptides in plants for some applications. In order to accomplish this, a recombinant DNA construct designed for co-suppression of the instant polypeptide can be constructed by linking a gene or gene fragment encoding that polypeptide to plant promoter sequences. Alternatively, a recombinant DNA construct designed to express antisense RNA for all or part of the instant nucleic acid fragment can be constructed by linking the gene or gene fragment in reverse orientation to plant promoter sequences. Either the co-suppression or antisense recombinant DNA constructs could be introduced into plants via transformation wherein expression of the corresponding endogenous genes are reduced or eliminated.

[0060] Molecular genetic solutions to the generation of plants with altered gene expression have a decided advantage over more traditional plant breeding approaches. Changes in plant phenotypes can be produced by specifically inhibiting expression of one or more genes by antisense inhibition or cosuppression (U.S. Pat. Nos. 5,190,931, 5,107,065 and 5,283,323). An antisense or cosuppression construct would act as a dominant negative regulator of gene activity. While conventional mutations can yield negative regulation of gene activity these effects are most likely recessive. The dominant negative regulation available with a transgenic approach may be advantageous from a breeding perspective. In addition, the ability to restrict the expression of a specific phenotype to the reproductive tissues of the plant by the use of tissue specific promoters may confer agronomic advantages relative to conventional mutations which may have an effect in all tissues in which a mutant gene is ordinarily expressed.

[0061] The person skilled in the art will know that special considerations are associated with the use of antisense or cosuppression technologies in order to reduce expression of particular genes. For example, the proper level of expression of sense or antisense genes may require the use of different recombinant DNA constructs utilizing different regulatory elements known to the skilled artisan. Once transgenic plants are obtained by one of the methods described above, it will be necessary to screen individual transgenics for those that most effectively display the desired phenotype. Accordingly, the skilled artisan will develop methods for screening large numbers of transformants. The nature of these screens will generally be chosen on practical grounds. For example, one can screen by looking for changes in gene expression by using antibodies specific for the protein encoded by the gene being suppressed, or one could establish assays that specifically measure enzyme activity. A preferred method will be one which allows large numbers of samples to be processed rapidly, since it will be expected that a large number of transformants will be negative for the desired phenotype.

[0062] In another embodiment, the present invention includes a phospholipid:diacylglycerol acyltransferase (PDAT) polypeptide having an amino acid sequence that is at least 80% identical, based on the Clustal V method of alignment, to a polypeptide selected from the group consisting of SEQ ID NO:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 32, 34 or 36.

[0063] The instant polypeptides (or portions thereof may be produced in heterologous host cells, particularly in the cells of microbial hosts, and can be used to prepare antibodies to these proteins by methods well known to those skilled in the art. The antibodies are useful for detecting the polypeptides of the instant invention in situ in cells or in vitro in cell extracts. Preferred heterologous host cells for production of the instant polypeptides are microbial hosts. Microbial expression systems and expression vectors containing regulatory sequences that direct high level expression of foreign proteins are well known to those skilled in the art. Any of these could be used to construct a recombinant DNA construct for production of the instant polypeptides. This recombinant DNA construct could then be introduced into appropriate microorganisms via transformation to provide high level expression of the encoded phospholipid:diacylglycerol acyltransferase. An example of a vector for high level expression of the instant polypeptides in a bacterial host is provided (Example 7).

[0064] All or a substantial portion of the polynucleotides of the instant invention may also be used as probes for genetically and physically mapping the genes that they are a part of, and used as markers for traits linked to those genes. Such information may be useful in plant breeding in order to develop lines with desired phenotypes. For example, the instant nucleic acid fragments may be used as restriction fragment length polymorphism (RFLP) markers. Southern blots (Maniatis) of restriction-digested plant genomic DNA may be probed with the nucleic acid fragments of the instant invention. The resulting banding patterns may then be subjected to genetic analyses using computer programs such as MapMaker (Lander et al. (1987) Genomics 1:174-181) in order to construct a genetic map. In addition, the nucleic acid fragments of the instant invention may be used to probe Southern blots containing restriction endonuclease-treated genomic DNAs of a set of individuals representing parent and progeny of a defined genetic cross. Segregation of the DNA polymorphisms is noted and used to calculate the position of the instant nucleic acid sequence in the genetic map previously obtained using this population (Botstein et al. (1980) Am. J. Hum. Genet. 32:314-331).

[0065] The production and use of plant gene-derived probes for use in genetic mapping is described in Bernatzky and Tanksley (1986) Plant Mol. Biol. Reporter 4:37-41. Numerous publications describe genetic mapping of specific cDNA clones using the methodology outlined above or variations thereof. For example, F2 intercross populations, backcross populations, randomly mated populations, near isogenic lines, and other sets of individuals may be used for mapping. Such methodologies are well known to those skilled in the art.

[0066] Nucleic acid probes derived from the instant nucleic acid sequences may also be used for physical mapping (i.e., placement of sequences on physical maps; see Hoheisel et al. In: Nonmammalian Genomic Analysis: A Practical Guide, Academic press 1996, pp. 319-346, and references cited therein).

[0067] Nucleic acid probes derived from the instant nucleic acid sequences may be used in direct fluorescence in situ hybridization (FISH) mapping (Trask (1991) Trends Genet. 7:149-154). Although current methods of FISH mapping favor use of large clones (several to several hundred KB; see Laan et al. (1995) Genome Res. 5:13-20), improvements in sensitivity may allow performance of FISH mapping using shorter probes.

[0068] A variety of nucleic acid amplification-based methods of genetic and physical mapping may be carried out using the instant nucleic acid sequences. Examples include allele-specific amplification (Kazazian (1989) J. Lab. Clin. Med. 11:95-96), polymorphism of PCR-amplified fragments (CAPS; Sheffield et al. (1993) Genomics 16:325-332), allele-specific ligation (Landegren et al. (1988) Science 241:1077-1080), nucleotide extension reactions (Sokolov (1990) Nucleic Acid Res. 18:3671), Radiation Hybrid Mapping (Walter et al. (1997) Nat. Genet. 7:22-28) and Happy Mapping (Dear and Cook (1989) Nucleic Acid Res. 17:6795-6807). For these methods, the sequence of a nucleic acid fragment is used to design and produce primer pairs for use in the amplification reaction or in primer extension reactions. The design of such primers is well known to those skilled in the art. In methods employing PCR-based genetic mapping, it may be necessary to identify DNA sequence differences between the parents of the mapping cross in the region corresponding to the instant nucleic acid sequence. This, however, is generally not necessary for mapping methods.

[0069] Loss of function mutant phenotypes may be identified for the instant cDNA clones either by targeted gene disruption protocols or by identifying specific mutants for these genes contained in a maize population carrying mutations in all possible genes (Ballinger and Benzer (1989) Proc. Natl. Acad. Sci USA 86:9402-9406; Koes et al. (1995) Proc. Natl. Acad. Sci USA 92:8149-8153; Bensen et al. (1995) Plant Cell 7:75-84). The latter approach may be accomplished in two ways. First, short segments of the instant nucleic acid fragments may be used in polymerase chain reaction protocols in conjunction with a mutation tag sequence primer on DNAs prepared from a population of plants in which Mutator transposons or some other mutation-causing DNA element has been introduced (see Bensen, supra). The amplification of a specific DNA fragment with these primers indicates the insertion of the mutation tag element in or near the plant gene encoding the instant polypeptides. Alternatively, the instant nucleic acid fragment may be used as a hybridization probe against PCR amplification products generated from the mutation population using the mutation tag sequence primer in conjunction with an arbitrary genomic site primer, such as that for a restriction enzyme site-anchored synthetic adaptor. With either method, a plant containing a mutation in the endogenous gene encoding the instant polypeptides can be identified and obtained. This mutant plant can then be used to determine or confirm the natural function of the instant polypeptides disclosed herein.

EXAMPLES

[0070] The present invention is further illustrated in the following Examples, in which parts and percentages are by weight and degrees are Celsius, unless otherwise stated. It should be understood that these Examples, while indicating preferred embodiments of the invention, are given by way of illustration only. From the above discussion and these Examples, one skilled in the art can ascertain the essential characteristics of this invention, and without departing from the spirit and scope thereof, can make various changes and modifications of the invention to adapt it to various usages and conditions. Thus, various modifications of the invention in addition to those shown and described herein will be apparent to those skilled in the art from the foregoing description. Such modifications are also intended to fall within the scope of the appended claims.

Example 1

[0071] Composition of cDNA Libraries; Isolation and Sequencing of cDNA Clones

[0072] cDNA libraries representing mRNAs from various balsam pear (Momordica charantia), pot marigold (Calendula officinalis), eucalyptus (Eucalyptus grandis), grape (Vitis sp.), rice (Oryza sativa), vernonia (Vernonia mespilifolia), wheat-common (Triticum aestivum), guar (Cyamopsos tetragonoloba), guayule (Parthenium argentatum Grey), maize (Zea mays), rice (Oryza sativa), soybean (Glycine max) and sunflower (Helianthus sp.) tissues were prepared. The characteristics of the libraries are described below. TABLE 2 cDNA Libraries from Balsam Pear, Pot marigold, Eucalyptus, Grape, Rice, Vernonia, Wheat, Guar, Guayule, Maize, Rice, Soybean and Sunflower Library Tissue Clone fds Momordica charantia developing seed fds.pk0003.b4:fis ecs1c Pot marigold (Calendula officinalis) developing ecs1c.pk009.j18:fis seeds eef1c Eucalyptus tereticornis flower buds from adult tree eef1c.pk006.c14:fis vmb1na Grape (Vitis sp.) midstage berries normalized vmb1na.pk016.c2:fis rsr9n Rice (Oryza sative L.) leaf 15 days after rsr9n.pk002.f3:fis germination harvested 2-72 hours following infection with Magnaporta grisea* vs1n Vernonia Seed* vs1n.pk016.n3:fis wpa1c Wheat (Triticum aestivum) pre-meiotic anthers JIC wpa1c.pk009.g15 wpa1c.pk009.g15:fis lds3c Guar (Cyamopsos tetragonoloba) seeds harvested lds3c.pk001.j8:fis 32 days after flowering lds3c.pk008.f17:fis epb3c Guayule (Parthenium argentatum, 11591) stem epb3c.pk008.j11:fis bark harvested at Dec. 28, 1993 - high activity for rubber biosynthesis cds2f Corn (Zea mays, B73) 11 day old seedling full cds2f.pk002.k4:fis length library using trehalose rlr6 Rice leaf 15 days after germination, 6 hours after rlr6.pk0092.c4:fis infection of strain with Magaporthe grisea; Resistant sdp2c Soybean (Glycine max L.) developing pods (6-7 sdp2c.pk034.e7:fis mm) sgs4c Soybean (Glycine max L.) seeds 2 days after sgs4c.pk006.b20:fis germination hlp1c Sunflower (Helianthus sp.) leaf infected with hlp1c.pk004.i1:fis phomopsis wip1c Wheat (Triticum aestivum, Hi Line) immature pistils wip1c.pk005.b24:fis wlm96 Wheat (Wheat aestivum) seedlings 96 hours after wlm96.pk0006.f11 inoculation with Erysiphe graminis f. sp tritici

[0073] CDNA libraries may be prepared by any one of many methods available. For example, the cDNAs may be introduced into plasmid vectors by first preparing the cDNA libraries in Uni-ZAP™ XR vectors according to the manufacturer's protocol (Stratagene Cloning Systems, La Jolla, Calif.). The Uni-ZAP™ XR libraries are converted into plasmid libraries according to the protocol provided by Stratagene. Upon conversion, cDNA inserts will be contained in the plasmid vector pBluescript. In addition, the cDNAs may be introduced directly into precut Bluescript II SK(+) vectors (Stratagene) using T4 DNA ligase (New England Biolabs), followed by transfection into DH10B cells according to the manufacturer's protocol (GIBCO BRL Products). Once the cDNA inserts are in plasmid vectors, plasmid DNAs are prepared from randomly picked bacterial colonies containing recombinant pBluescript plasmids, or the insert cDNA sequences are amplified via polymerase chain reaction using primers specific for vector sequences flanking the inserted cDNA sequences. Amplified insert DNAs or plasmid DNAs are sequenced in dye-primer sequencing reactions to generate partial cDNA sequences (expressed sequence tags or “ESTs”; see Adams et al., (1991) Science 252:1651-1656). The resulting ESTs are analyzed using a Perkin Elmer Model 377 fluorescent sequencer.

[0074] Full-insert sequence (FIS) data is generated utilizing a modified transposition protocol. Clones identified for FIS are recovered from archived glycerol stocks as single colonies, and plasmid DNAs are isolated via alkaline lysis. Isolated DNA templates are reacted with vector primed M13 forward and reverse oligonucleotides in a PCR-based sequencing reaction and loaded onto automated sequencers. Confirmation of clone identification is performed by sequence alignment to the original EST sequence from which the FIS request is made.

[0075] Confirmed templates are transposed via the Primer Island transposition kit (PE Applied Biosystems, Foster City, Calif.) which is based upon the Saccharomyces cerevisiae Ty1 transposable element (Devine and Boeke (1994) Nucleic Acids Res. 22:3765-3772). The in vitro transposition system places unique binding sites randomly throughout a population of large DNA molecules. The transposed DNA is then used to transform DH10B electro-competent cells (Gibco BRL/Life Technologies, Rockville, Md.) via electroporation. The transposable element contains an additional selectable marker (named DHFR; Fling and Richards (1983) Nucleic Acids Res. 11:5147-5158), allowing for dual selection on agar plates of only those subclones containing the integrated transposon. Multiple subclones are randomly selected from each transposition reaction, plasmid DNAs are prepared via alkaline lysis, and templates are sequenced (ABI Prism dye-terminator ReadyReaction mix) outward from the transposition event site, utilizing unique primers specific to the binding sites within the transposon.

[0076] Sequence data is collected (ABI Prism Collections) and assembled using Phred/Phrap (P. Green, University of Washington, Seattle). Phrep/Phrap is a public domain software program which re-reads the ABI sequence data, re-calls the bases, assigns quality values, and writes the base calls and quality values into editable output files. The Phrap sequence assembly program uses these quality values to increase the accuracy of the assembled sequence contigs. Assemblies are viewed by the Consed sequence editor (D. Gordon, University of Washington, Seattle).

[0077] In some of the clones the cDNA fragment corresponds to a portion of the 3′-terminus of the gene and does not cover the entire open reading frame. In order to obtain the upstream information one of two different protocols are used. The first of these methods results in the production of a fragment of DNA containing a portion of the desired gene sequence while the second method results in the production of a fragment containing the entire open reading frame. Both of these methods use two rounds of PCR amplification to obtain fragments from one or more libraries. The libraries some times are chosen based on previous knowledge that the specific gene should be found in a certain tissue and some times are randomly-chosen. Reactions to obtain the same gene may be performed on several libraries in parallel or on a pool of libraries. Library pools are normally prepared using from 3 to 5 different libraries and normalized to a uniform dilution. In the first round of amplification both methods use a vector-specific (forward) primer corresponding to a portion of the vector located at the 5′-terminus of the clone coupled with a gene-specific (reverse) primer. The first method uses a sequence that is complementary to a portion of the already known gene sequence while the second method uses a gene-specific primer complementary to a portion of the 3′-untranslated region (also referred to as UTR). In the second round of amplification a nested set of primers is used for both methods. The resulting DNA fragment is ligated into a pBluescript vector using a commercial kit and following the manufacturer's protocol. This kit is selected from many available from several vendors including Invitrogen (Carlsbad, Calif.), Promega Biotech (Madison, Wis.), and Gibco-BRL (Gaithersburg, Md.). The plasmid DNA is isolated by alkaline lysis method and submitted for sequencing and assembly using Phred/Phrap, as above.

Example 2

[0078] Identification of cDNA Clones

[0079] cDNA clones encoding phospholipid:diacylglycerol acyltransferases were identified by conducting BLAST (Basic Local Alignment Search Tool; Altschul et al. (1993) J. Mol. Biol. 215:403-410; see also the explanation of the BLAST alogarithm on the world wide web site for the National Center for Biotechnology Information at the National Library of Medicine of the National Institutes of Health) searches for similarity to sequences contained in the BLAST “nr” database (comprising all non-redundant GenBank CDS translations, sequences derived from the 3-dimensional structure Brookhaven Protein Data Bank, the last major release of the SWISS-PROT protein sequence database, EMBL, and DDBJ databases). The cDNA sequences obtained in Example 1 were analyzed for similarity to all publicly available DNA sequences contained in the “nr” database using the BLASTN algorithm provided by the National Center for Biotechnology Information (NCBI). The DNA sequences were translated in all reading frames and compared for similarity to all publicly available protein sequences contained in the “nr” database using the BLASTX algorithm (Gish and States (1993) Nat. Genet. 3:266-272) provided by the NCBI. For convenience, the P-value (probability) of observing a match of a cDNA sequence to a sequence contained in the searched databases merely by chance as calculated by BLAST are reported herein as “pLog” values, which represent the negative of the logarithm of the reported P-value. Accordingly, the greater the pLog value, the greater the likelihood that the cDNA sequence and the BLAST “hit” represent homologous proteins.

[0080] ESTs submitted for analysis are compared to the GenBank database as described above. ESTs that contain sequences more 5- or 3-prime can be found by using the BLASTn algorithm (Altschul et al (1997) Nucleic Acids Res. 25:3389-3402.) against the DuPont proprietary database comparing nucleotide sequences that share common or overlapping regions of sequence homology. Where common or overlapping sequences exist between two or more nucleic acid fragments, the sequences can be assembled into a single contiguous nucleotide sequence, thus extending the original fragment in either the 5 or 3 prime direction. Once the most 5-prime EST is identified, its complete sequence can be determined by Full Insert Sequencing as described in Example 1. Homologous genes belonging to different species can be found by comparing the amino acid sequence of a known gene (from either a proprietary source or a public database) against an EST database using the tBLASTn algorithm. The tBLASTn algorithm searches an amino acid query against a nucleotide database that is translated in all 6 reading frames. This search allows for differences in nucleotide codon usage between different species, and for codon degeneracy.

Example 3

[0081] Characterization of cDNA Clones Encoding Proteins Similar to Arabidopsis thaliana PDAT 2

[0082] The BLASTX search using the EST sequences from clones listed in Table 3 revealed similarity of the polypeptides encoded by the cDNAs to phospholipid:diacylglycerol acyltransferase (PDAT) 2 from Arabidopsis thaliana (NCBI General Identifier No. 15240676; SEQ ID NO:30) (NCBI General Identifier No. 15240676 is 100% identical to NCBI General Identifier No. 9758029.) Shown in Table 3 are the Blast results for the sequences of the entire cDNA inserts comprising the indicated cDNA clones (“FIS”), the sequences of contigs assembled from two or more ESTs (“Contig”), sequences of contigs assembled from an FIS and one or more ESTs (“Contig*”) or sequences encoding an entire protein derived from an FIS, a contig, or an FIS and PCR (“CGS”): TABLE 3 BLAST Results for Sequences Encoding Polypeptides Homologous to Phospholipid:diacylglycerol Acyltransferase (PDAT) 2 BLAST pLog Score Clone Status NCBI General Identifier No. 15240676 lds3c.pk001.j8:fis FIS 165.00 epb3c.pk008.j11:fis CGS 180.00 Contig of: CGS 180.00 cds2f.pk002.k4:fis rlr6.pk0092.c4:fis CGS 180.00 sdp2c.pk034.e7:fis CGS 180.00 hlp1c.pk004.i1:fis CGS 180.00 Contig of: Contig 180.00 wip1c.pk005.b24:fis wlm96.pk0006.f11 sgs4c.pk006.b20:fis CGS 180.00

[0083] The nucleotide sequence of the entire cDNA insert in clone lds3c.pk001.j8:fis is shown in SEQ ID NO:15. The amino acid sequence deduced from nucleotides 10 through 1176 of SEQ ID NO:15 is shown in SEQ ID NO:16 (stop codon encoded by nucleotides 1177-1179). The nucleotide sequence of the entire cDNA insert in clone epb3c.pk008.j11:fis is shown in SEQ ID NO:17. The amino acid sequence deduced from nucleotides 39 through 2042 of SEQ ID NO:17 is shown in SEQ ID NO:18 (start codon encoded by nucleotides 39-41 and stop codon encoded by nucleotides 2043-2045). The nucleotide sequence of the contig of clone cds2f.pk002.k4:fis is shown in SEQ ID NO:19. The amino acid sequence deduced from nucleotides 202 through 2229 of SEQ ID NO:19 is shown in SEQ ID NO:20 (start codon encoded by nucleotides 202-204 and stop codon encoded by nucleotides 2230-2232). The nucleotide sequence of the entire cDNA insert in clone rlr6.pk0092.c4:fis is shown in SEQ ID NO:21. The amino acid sequence deduced from nucleotides 160 through 2232 of SEQ ID NO:21 is shown in SEQ ID NO:22 (start codon encoded by nucleotides 160-162 and stop codon encoded by nucleotides 2233-2235). The nucleotide sequence of the entire cDNA insert in clone sdp2c.pk034.e7:fis is shown in SEQ ID NO:23. The amino acid sequence deduced from nucleotides 330 through 2357 of SEQ ID NO:23 is shown in SEQ ID NO:24 (start codon encoded by nucleotides 330-332 and stop codon encoded by nucleotides 2358-2360). The nucleotide sequence of the entire cDNA insert in clone hlp1c.pk004.i1:fis is shown in SEQ ID NO:25. The amino acid sequence deduced from nucleotides 104 through 2113 of SEQ ID NO:25 is shown in SEQ ID NO:26 (start codon encoded by nucleotides 104-106 and stop codon encoded by nucleotides 2114-2116). The nucleotide sequence of the contig of clones wip1c.pk005:b24:fis and wlm96.pk0006.f11 is shown in SEQ ID NO:27. The amino acid sequence of SEQ ID NO:27 is shown in SEQ ID NO:28 (stop codon encoded by nucleotides 1801-1803). The nucleotide sequence of the entire cDNA insert in clone sgs4c.pk006.b20:fis is shown in SEQ ID NO:35. The amino acid sequence deduced from nucleotides 267 through 2294 of SEQ ID NO:35 is shown in SEQ ID NO:36 (start codon encoded by nucleotides 267-269 and stop codon encoded by nucleotides 2295-2297).

[0084]FIGS. 1A, 1B, 1C, 1D, 1E and 1F present an alignment of the amino acid sequences set forth in SEQ ID NOs:16, 18, 20, 22, 24, 26, 28, 36 and the sequence from Arabidopsis thaliana sequence (NCBI General Identification (GI) No. 15240676; SEQ ID NO:30). The data in Table 4 represents a calculation of the percent identity of the amino acid sequences set forth in SEQ ID NOs: 16, 18, 20, 22, 24, 26, 28, 36 and the sequence from Arabidopsis thaliana sequence (NCBI General Identification (GI) No. 15240676; SEQ ID NO:30). TABLE 4 Percent Identity of Amino Acid Sequences Deduced From the Nucleotide Sequences of cDNA Clones Encoding Polypeptides Homologous to Phospholipid:diacylglycerol Acyltransferase (PDAT) 2 Percent Identity to NCBI General Identifier No. 15240676 Clone SEQ ID NO. (SEQ ID NO: 30) lds3c.pk001.j8:fis 16 71.2 epb3c.pk008.j11:fis 18 74.0 Contig of: 20 73.3 cds2f.pk002.k4:fis rlr6.pk0092.c4:fis 22 73.2 sdp2c.pk034.e7:fis 24 71.8 hlp1c.pk004.i1:fis 26 74.6 Contig of: 28 74.2 wip1c.pk005.b24:fis wlm96.pk0006.f11 sgs4c.pk006.b20:fis 36 72.3

[0085] Sequence alignments and percent identity calculations were performed using the Megalign program of the LASERGENE bioinformatics computing suite (DNASTAR Inc., Madison, Wis.). Multiple alignment of the sequences was performed using the Clustal V method of alignment (Higgins and Sharp (1989) CABIOS. 5:151-153) with the default parameters (GAP PENALTY=10, GAP LENGTH PENALTY=10). Default parameters for pairwise alignments using the Clustal V method of alignment were KTUPLE 1, GAP PENALTY=3, WINDOW=5 and DIAGONALS SAVED=5. Sequence alignments and BLAST scores and probabilities indicate that the nucleic acid fragments comprising the instant cDNA clones encode a substantial portion of a phospholipid:diacylglycerol acyltransferase. These sequences are believed to represent the first dicot species sequences encoding phospholipid:diacylglycerol acyltransferases known to Applicant.

Example 4

[0086] Characterization of cDNA Clones Encoding Proteins Similar to Arabidopsis thaliana PDAT 1

[0087] The BLASTX search using the EST sequences from clones listed in Table 5 revealed similarity of the polypeptides encoded by the cDNAs to phospholipid:diacylglycerol acyltransferase (PDAT) 1 from Arabidopsis thaliana (NCBI General Identifier No. 7452457; SEQ ID NO:29). (NCBI General Identifier No. 7452457 is 100% identical to NCBI General Identifier No. 15235214.) Shown in Table 5 are the BLAST results for the sequences of the entire cDNA inserts comprising the indicated cDNA clones (“FIS”), the sequences of contigs assembled from two or more ESTs (“Contig”), sequences of contigs assembled from an FIS and one or more ESTs (“Contig*”) or sequences encoding an entire protein derived from an FIS, a contig, or an FIS and PCR (“CGS”): TABLE 5 BLAST Results for Sequences Encoding Polypeptides Homologous to Phospholipid:diacylglycerol Acyltransferase (PDAT) 1 BLAST pLog Score NCBI General Identifier No. 7452457 Clone Status (SEQ ID NO: 29) fds.pk0003.b4:fis CGS 90.30 ecs1c.pk009.j18:fis CGS 90.70 eef1c.pk006.c14:fis CGS 146.00 vmb1na.pk016.c2:fis CGS 99.00 rsr9n.pk002.f3:fis FIS 45.52 vs1n.pk016.n3:fis FIS 47.70 wpa1c.pk009.g15 EST 42.70 lds3c.pk008.f17:fis CGS 89.05 wpa1c.pk009.g15:fis CGS 84.52

[0088] The nucleotide sequence of the entire cDNA insert in clone fds.pk0003.b4:fis is shown in SEQ ID NO:1. The amino acid sequence deduced from nucleotides 72 through 1682 of SEQ ID NO:1 is shown in SEQ ID NO:2 (start codon encoded by nucleotides 72-74 and stop codon encoded by nucleotides 1683-1685). The nucleotide sequence of the entire cDNA insert in clone ecs1c.pk009.j18:fis is shown in SEQ ID NO:3. The amino acid sequence deduced from nucleotides 29 through 1618 of SEQ ID NO:3 is shown in SEQ ID NO:4 (start codon encoded by nucleotides 29-31 and stop codon encoded by nucleotides 1619-1621). The nucleotide sequence of the entire cDNA insert in clone eef1c.pk006.c14:fis is shown in SEQ ID NO:5. The amino acid sequence deduced from nucleotides 216 through 1820 of SEQ ID NO:5 is shown in SEQ ID NO:6 (start codon encoded by nucleotides 216-218 and stop codon encoded by nucleotides 1821-1823). The nucleotide sequence of the entire cDNA insert in clone vmb1na.pk016.c2:fis is shown in SEQ ID NO:7. The amino acid sequence deduced from nucleotides 202 through 1800 of SEQ ID NO:7 is shown in SEQ ID NO:8 (start codon encoded by nucleotides 202-204 and stop codon encoded by nucleotides 1801-1803). The nucleotide sequence of the entire cDNA insert in clone rsr9n.pk002.f3:fis is shown in SEQ ID NO:9. The amino acid sequence deduced from nucleotides 2 through 1213 of SEQ ID NO:9 is shown in SEQ ID NO:10 (stop codon encoded by nucleotides 1214-1216). The nucleotide sequence of the contig of clone vs1n.pk016.n3:fis is shown in SEQ ID NO:11. The amino acid sequence deduced from nucleotides 2 through 1300 of SEQ ID NO:11 is shown in SEQ ID NO:12 (stop codon encoded by nucleotides 1301-1303). The nucleotide sequence of a portion of the cDNA insert in clone wpa1c.pk009.g15 is shown in SEQ ID NO:13. The amino acid sequence deduced from nucleotides 238 through 634 of SEQ ID NO:13 is shown in SEQ ID NO:14 (start codon encoded by nucleotides 238-240). The nucleotide sequence of the entire cDNA insert in clone lds3c.pk008.f17:fis is shown in SEQ ID NO:31. The amino acid sequence deduced from nucleotides 125 through 1741 of SEQ ID NO:31 is shown in SEQ ID NO:32 (start codon encoded by nucleotides 125-127 and stop codon encoded by nucleotides 1739-1741). The nucleotide sequence of the entire cDNA insert in clone wpa1c.pk009.g15:fis is shown in SEQ ID NO:33. The amino acid sequence deduced from nucleotides 238 through 1839 of SEQ ID NO:33 is shown in SEQ ID NO:34 (start codon encoded by nucleotides 238-240 and stop codon encoded by nucleotides 1840-1842).

[0089]FIGS. 2A, 2B, 2C, 2D and 2E present an alignment of the amino acid sequences set forth in SEQ ID NOs:2, 4, 6, 8, 10, 12, 14, 32, 34 and the sequence from Arabidopsis thaliana sequence (NCBI General Identification (GI) No. 7452457; SEQ ID NO:29). The data in Table 6 represents a calculation of the percent identity of the amino acid sequences set forth in SEQ ID NOs: 2, 4, 6, 8, 10, 12, 14, 32, 34 and the sequence from Arabidopsis thaliana sequence (NCBI General Identification (GI) No. 7452457; SEQ ID NO:29). TABLE 6 Percent Identity of Amino Acid Sequences Deduced From the Nucleotide Sequences of cDNA Clones Encoding Polypeptides Homologous to Phospholipid:diacylglycerol Acyltransferase (PDAT) 1 Percent Identity to SEQ ID NCBI General Identifier No. 7452457; Clone NO. SEQ ID NO: 29 fds.pk0003.b4:fis 2 52.1 ecs1c.pk009.j18:fis 4 48.3 eef1c.pk006.c14:fis 6 56.2 vmb1na.pk016.c2:fis 8 54.4 rsr9n.pk002.f3:fis 10 39.1 vs1n.pk016.n3:fis 12 43.0 wpa1c.pk009.g15 14 58.3 lds3c.pk008.f17:fis 32 52.5 wpa1c.pk009.g15:fis 34 47.7

[0090] Sequence alignments and percent identity calculations were performed using the Megalign program of the LASERGENE bioinformatics computing suite (DNASTAR Inc., Madison, Wis.). Multiple alignment of the sequences was performed using the Clustal V method of alignment (Higgins and Sharp (1989) CABIOS. 5:151-153) with the default parameters (GAP PENALTY=10, GAP LENGTH PENALTY=10). Default parameters for pairwise alignments using the Clustal V method of alignment were KTUPLE 1, GAP PENALTY=3, WINDOW=5 and DIAGONALS SAVED=5. Sequence alignments and BLAST scores and probabilities indicate that the nucleic acid fragments comprising the instant cDNA clones encode a substantial portion of a phospholipid:diacylglycerol acyltransferase.

Example 5

[0091] Expression of Recombinant DNA Constructs in Monocot Cells

[0092] A recombinant DNA construct comprising a cDNA encoding the instant polypeptides in sense orientation with respect to the maize 27 kD zein promoter that is located 5′ to the cDNA fragment, and the 10 kD zein 3′ end that is located 3′ to the cDNA fragment, can be constructed. The cDNA fragment of this gene may be generated by polymerase chain reaction (PCR) of the cDNA clone using appropriate oligonucleotide primers. Cloning sites (Ncol or Smal) can be incorporated into the oligonucleotides to provide proper orientation of the DNA fragment when inserted into the digested vector pML 103 as described below. Amplification is then performed in a standard PCR. The amplified DNA is then digested with restriction enzymes Ncol and Smal and fractionated on an agarose gel. The appropriate band can be isolated from the gel and combined with a 4.9 kb Ncol-Smal fragment of the plasmid pML 103. Plasmid pML 103 has been deposited under the terms of the Budapest Treaty at ATCC (American Type Culture Collection, 10801 University Blvd., Manassas, Va. 20110-2209), and bears accession number ATCC 97366. The DNA segment from pML 103 contains a 1.05 kb Sall-Ncol promoter fragment of the maize 27 kD zein gene and a 0.96 kb Smal-Sall fragment from the 3′ end of the maize 10 kD zein gene in the vector pGem9Zf(+) (Promega). Vector and insert DNA can be ligated at 15° C. overnight, essentially as described (Maniatis). The ligated DNA may then be used to transform E. coli XL-1-Blue (Epicurian Coli XL-1 Blue™; Stratagene). Bacterial transformants can be screened by restriction enzyme digestion of plasmid DNA and limited nucleotide sequence analysis using the dideoxy chain termination method (Sequenase™ DNA Sequencing Kit; U.S. Biochemical). The resulting plasmid construct would comprise a recombinant DNA construct encoding, in the 5′ to 3′ direction, the maize 27 kD zein promoter, a cDNA fragment encoding the instant polypeptides, and the 10-kD zein 3′ region.

[0093] The recombinant DNA construct described above can then be introduced into corn cells by the following procedure. Immature corn embryos can be dissected from developing caryopses derived from crosses of the inbred corn lines H99 and LH132. The embryos are isolated 10 to 11 days after pollination when they are 1.0 to 1.5 mm long. The embryos are then placed with the axis-side facing down and in contact with agarose-solidified N6 medium (Chu et al. (1975) Sci. Sin. Peking 18:659-668). The embryos are kept in the dark at 27° C. Friable embryogenic callus consisting of undifferentiated masses of cells with somatic proembryoids and embryoids borne on suspensor structures proliferates from the scutellum of these immature embryos. The embryogenic callus isolated from the primary explant can be cultured on N6 medium and sub-cultured on this medium every 2 to 3 weeks.

[0094] The plasmid, p35S/Ac (obtained from Dr. Peter Eckes, Hoechst Ag, Frankfurt, Germany) may be used in transformation experiments in order to provide for a selectable marker. This plasmid contains the Pat gene (see European Patent Publication 0 242 236) which encodes phosphinothricin acetyl transferase (PAT). The enzyme PAT confers resistance to herbicidal glutamine synthetase inhibitors such as phosphinothricin. The pat gene in p35S/Ac is under the control of the 35S promoter from Cauliflower Mosaic Virus (Odell et al. (1985) Nature 313:810-812) and the 3′ region of the nopaline synthase gene from the T-DNA of the Ti plasmid of Agrobacterium tumefaciens.

[0095] The particle bombardment method (Klein et al. (1987) Nature 327:70-73) may be used to transfer genes to the callus culture cells. According to this method, gold particles (1 μm in diameter) are coated with DNA using the following technique. Ten μg of plasmid DNAs are added to 50 μL of a suspension of gold particles (60 mg per mL). Calcium chloride (50 μL of a 2.5 M solution) and spermidine free base (20 μL of a 1.0 M solution) are added to the particles. The suspension is vortexed during the addition of these solutions. After 10 minutes, the tubes are briefly centrifuged (5 sec at 15,000 rpm) and the supernatant removed. The particles are resuspended in 200 μL of absolute ethanol, centrifuged again and the supernatant removed. The ethanol rinse is performed again and the particles resuspended in a final volume of 30 μL of ethanol. An aliquot (5 μL) of the DNA-coated gold particles can be placed in the center of a Kapton™ flying disc (Bio-Rad Labs). The particles are then accelerated into the corn tissue with a Biolistic™ PDS-1000/He (Bio-Rad Instruments, Hercules Calif.), using a helium pressure of 1000 psi, a gap distance of 0.5 cm and a flying distance of 1.0 cm.

[0096] For bombardment, the embryogenic tissue is placed on filter paper over agarose-solidified N6 medium. The tissue is arranged as a thin lawn and covered a circular area of about 5 cm in diameter. The petri dish containing the tissue can be placed in the chamber of the PDS-1000/He approximately 8 cm from the stopping screen. The air in the chamber is then evacuated to a vacuum of 28 inches of Hg. The macrocarrier is accelerated with a helium shock wave using a rupture membrane that bursts when the He pressure in the shock tube reaches 1000 psi.

[0097] Seven days after bombardment the tissue can be transferred to N6 medium that contains bialophos (5 mg per liter) and lacks casein or proline. The tissue continues to grow slowly on this medium. After an additional 2 weeks the tissue can be transferred to fresh N6 medium containing bialophos. After 6 weeks, areas of about 1 cm in diameter of actively growing callus can be identified on some of the plates containing the bialophos-supplemented medium. These calli may continue to grow when sub-cultured on the selective medium.

[0098] Plants can be regenerated from the transgenic callus by first transferring clusters of tissue to N6 medium supplemented with 0.2 mg per liter of 2,4-D. After two weeks the tissue can be transferred to regeneration medium (Fromm et al. (1990) Bio/Technology 8:833-839).

Example 6

[0099] Expression of Recombinant DNA Constructs in Dicot Cells

[0100] A seed-specific expression cassette composed of the promoter and transcription terminator from the gene encoding the β subunit of the seed storage protein phaseolin from the bean Phaseolus vulgaris (Doyle et al. (1986) J. Biol. Chem. 261:9228-9238) can be used for expression of the instant polypeptides in transformed soybean. The phaseolin cassette includes about 500 nucleotides upstream (5′) from the translation initiation codon and about 1650 nucleotides downstream (3′) from the translation stop codon of phaseolin. Between the 5′ and 3′ regions are the unique restriction endonuclease sites Ncol (which includes the ATG translation initiation codon), Smal, Kpnl and Xbal. The entire cassette is flanked by HindIII sites.

[0101] The cDNA fragment of this gene may be generated by polymerase chain reaction (PCR) of the cDNA clone using appropriate oligonucleotide primers. Cloning sites can be incorporated into the oligonucleotides to provide proper orientation of the DNA fragment when inserted into the expression vector. Amplification is then performed as described above, and the isolated fragment is inserted into a pUC18 vector carrying the seed expression cassette.

[0102] Soybean embryos may then be transformed with the expression vector comprising sequences encoding the instant polypeptides. To induce somatic embryos, cotyledons, 3-5 mm in length dissected from surface sterilized, immature seeds of the soybean cultivar A2872, can be cultured in the light or dark at 26° C. on an appropriate agar medium for 6-10 weeks. Somatic embryos which produce secondary embryos are then excised and placed into a suitable liquid medium. After repeated selection for clusters of somatic embryos which multiplied as early, globular staged embryos, the suspensions are maintained as described below.

[0103] Soybean embryogenic suspension cultures can be maintained in 35 mL liquid media on a rotary shaker, 150 rpm, at 26° C. with florescent lights on a 16:8 hour day/night schedule. Cultures are subcultured every two weeks by inoculating approximately 35 mg of tissue into 35 mL of liquid medium.

[0104] Soybean embryogenic suspension cultures may then be transformed by the method of particle gun bombardment (Klein et al. (1987) Nature (London) 327:70-73, U.S. Pat. No. 4,945,050). A DuPont Biolistic™ PDS1000/HE instrument (helium retrofit) can be used for these transformations.

[0105] A selectable marker gene which can be used to facilitate soybean transformation is a recombinant DNA construct composed of the 35S promoter from Cauliflower Mosaic Virus (Odell et al. (1985) Nature 313:810-812), the hygromycin phosphotransferase gene from plasmid pJR225 (from E. coli; Gritz et al. (1983) Gene 25:179-188) and the 3′ region of the nopaline synthase gene from the T-DNA of the Ti plasmid of Agrobacterium tumefaciens. The seed expression cassette comprising the phaseolin 5′ region, the fragment encoding the instant polypeptides and the phaseolin 3′ region can be isolated as a restriction fragment. This fragment can then be inserted into a unique restriction site of the vector carrying the marker gene.

[0106] To 50 μL of a 60 mg/mL 1 μm gold particle suspension is added (in order): 5 μL DNA (1 μg/μL), 20 μL spermidine (0.1 M), and 50 μL CaCl₂ (2.5 M). The particle preparation is then agitated for three minutes, spun in a microfuge for 10 seconds and the supernatant removed. The DNA-coated particles are then washed once in 400 μL 70% ethanol and resuspended in 40 μL of anhydrous ethanol. The DNA/particle suspension can be sonicated three times for one second each. Five μL of the DNA-coated gold particles are then loaded on each macro carrier disk.

[0107] Approximately 300-400 mg of a two-week-old suspension culture is placed in an empty 60×15 mm petri dish and the residual liquid removed from the tissue with a pipette. For each transformation experiment, approximately 5-10 plates of tissue are normally bombarded. Membrane rupture pressure is set at 1100 psi and the chamber is evacuated to a vacuum of 28 inches mercury. The tissue is placed approximately 3.5 inches away from the retaining screen and bombarded three times. Following bombardment, the tissue can be divided in half and placed back into liquid and cultured as described above.

[0108] Five to seven days post bombardment, the liquid media may be exchanged with fresh media, and eleven to twelve days post bombardment with fresh media containing 50 mg/mL hygromycin. This selective media can be refreshed weekly. Seven to eight weeks post bombardment, green, transformed tissue may be observed growing from untransformed, necrotic embryogenic clusters. Isolated green tissue is removed and inoculated into individual flasks to generate new, clonally propagated, transformed embryogenic suspension cultures. Each new line may be treated as an independent transformation event. These suspensions can then be subcultured and maintained as clusters of immature embryos or regenerated into whole plants by maturation and germination of individual somatic embryos.

Example 7

[0109] Expression of Recombinant DNA Constructs in Microbial Cells

[0110] The cDNAs encoding the instant polypeptides can be inserted into the T7 E. coli expression vector pBT430. This vector is a derivative of pET-3a (Rosenberg et al. (1987) Gene 56:125-135) which employs the bacteriophage T7 RNA polymerase/T7 promoter system. Plasmid pBT430 was constructed by first destroying the EcoRI and HindIII sites in pET-3a at their original positions. An oligonucleotide adaptor containing EcoRI and Hind III sites was inserted at the BamHI site of pET-3a. This created pET-3aM with additional unique cloning sites for insertion of genes into the expression vector. Then, the Ndel site at the position of translation initiation was converted to an Ncol site using oligonucleotide-directed mutagenesis. The DNA sequence of pET-3aM in this region, 5′-CATATGG, was converted to 5′-CCCATGG in pBT430.

[0111] Plasmid DNA containing a cDNA may be appropriately digested to release a nucleic acid fragment encoding the protein. This fragment may then be purified on a 1% low melting agarose gel. Buffer and agarose contain 10 μg/ml ethidium bromide for visualization of the DNA fragment. The fragment can then be purified from the agarose gel by digestion with GELase™ (Epicentre Technologies, Madison, Wis.) according to the manufacturer's instructions, ethanol precipitated, dried and resuspended in 20 μL of water. Appropriate oligonucleotide adapters may be ligated to the fragment using T4 DNA ligase (New England Biolabs (NEB), Beverly, Mass.). The fragment containing the ligated adapters can be purified from the excess adapters using low melting agarose as described above. The vector pBT430 is digested, dephosphorylated with alkaline phosphatase (NEB) and deproteinized with phenol/chloroform as described above. The prepared vector pBT430 and fragment can then be ligated at 16° C. for 15 hours followed by transformation into DH5 electrocompetent cells (GIBCO BRL). Transformants can be selected on agar plates containing LB media and 100 μg/mL ampicillin. Transformants containing the gene encoding the instant polypeptides are then screened for the correct orientation with respect to the T7 promoter by restriction enzyme analysis.

[0112] For high level expression, a plasmid clone with the cDNA insert in the correct orientation relative to the T7 promoter can be transformed into E. coli strain BL21 (DE3) (Studier et al. (1986) J. Mol. Biol. 189:113-130). Cultures are grown in LB medium containing ampicillin (100 mg/L) at 25° C. At an optical density at 600 nm of approximately 1, IPTG (isopropylthio-β-galactoside, the inducer) can be added to a final concentration of 0.4 mM and incubation can be continued for 3 h at 25° C. Cells are then harvested by centrifugation and re-suspended in 50 μL of 50 mM Tris-HCI at pH 8.0 containing 0.1 mM DTT and 0.2 mM phenyl methylsulfonyl fluoride. A small amount of 1 mm glass beads can be added and the mixture sonicated 3 times for about 5 seconds each time with a microprobe sonicator. The mixture is centrifuged and the protein concentration of the supernatant determined. One μg of protein from the soluble fraction of the culture can be separated by SDS-polyacrylamide gel electrophoresis. Gels can be observed for protein bands migrating at the expected molecular weight.

[0113] Crude, partially purified or purified enzyme, either alone or as a fusion protein, may be utilized in assays for the evaluation of compounds for their ability to inhibit enzymatic activation of the instant polypeptides disclosed herein. Assays may be conducted under well known experimental conditions which permit optimal enzymatic activity. For example, assays for phospholipid:diacylglycerol acyltransferase (PDAT) are presented by Dahlqvist et al., Proc. Natl. Acad. Sci. USA 97(12):6487-6492 (2000).

1 36 1 1982 DNA Momordica charantia 1 gcacgagccg tcttctcaca atttgggggt ccgatttcac ttgcgcttga cgttcgtggg 60 gtgggattcc tatggctgtg ctcctggagg agattgtgaa gtccgttgag ttgtggttga 120 ggctgatcaa gaagccccag ccgtacgtcg atcccaacct cgatccggtt cttctgattc 180 ccggagttgc agggtcgatt ttgaatgcgg taaatgagga caccggcagg gaggagcgtg 240 tttgggtcag gattttaggg gccgattcta agttccgaac tgagctctgg tctttttacg 300 attccgcttc tggtgagtct gtatgttttg atccgaagac caaaattaga gttcctgatg 360 agagaagtgg attgtatgca atagatattt tggaccctga cctgatgatc ggatgcgatt 420 ctatatacta tttccatgac atgattgttg aaatgaccaa gtggggtttt caagaaggaa 480 aaactctttt tggatttgga tacgattttc ggcaaagtaa caggttgcca gaatcattgg 540 atcgtttagc tgctaaactg gaggcagtat ttagtgcttc aggagggaaa aagattaata 600 ttataagtca ctctatgggt ggtcttttag tgaaatgctt catgtgcctg cgcagcgaaa 660 tctttgagaa gtatgtgcag aattggattg caattgctgc tccattccag ggtgcacctg 720 gatatgttac atctaccttt gtgaatggaa tgtcatttgt caacggatgg aaacagaact 780 tctttatatc aaagtggagc atgcaccaac tgcttattga atgtccatcc atttacgaac 840 taatgggttc tccggacttt aattggcaac atattcctct tctagaaatc tggagacaga 900 aacatgatga cgatgggaac cctcacaatg tgttggaatc ttacctgctt aaagaaagtg 960 ttgaaatact gacagaatct ctttcaacaa acgcgattct tcatgatgga ttgactattc 1020 ccctgccatt taatttggag attttgaaat gggcaaacga gacacgggaa gttttaaaga 1080 atgctaaact tccttctcag gttaagtttt acaatatata tgcgacgggt cttgagacac 1140 cacatactgt ttgctatgga gatgcggaaa agccagttgc tgatttacat aatctacgat 1200 atattgagcc caattatatt tatgttgatg gtgatggcac ggttcctgtg gagtcggcaa 1260 aggctgatgg actcgatgca gtagcacgga tcggggtgcc cggtgagcac cagcgggttc 1320 ttagagacca ccgcgtcttc cggaggctca agcactggct caaggcaggt gatcctgatc 1380 ccttctatga cccgctaaac gactatgtga tcttgccaac agctttcgag gtcgaaagtc 1440 atgtggagaa aggtttgcaa gtagcagctc tgaaagagga atgggaaatc atctcccatg 1500 accaaaataa gacagatgag ttatgtaatg acaagccatt ggtgagttcc attatgctat 1560 ctcgagttac tgaggattgc ccgtcctcga gggccgaggc ttgcgcaact gttgtagttc 1620 atccccagca agacggtaag cagcacgtcg aactgaatgc tgttagtgta tcagttgatg 1680 catgaaagtg gcgcggcctg ttcttccaaa cccgactgca atcagcctca tgagcatttg 1740 ccattgatgc cgtttgatcg aatatctgta cagtcattat cacttgttta tgtggtgaga 1800 aatgtatatt aaaatttaga ttttctttta ttttttatta tttttttatg tatatagaag 1860 agacataact aaatgatcgt ttccttgcag tgctttaata atgggagaat ttaatcatgt 1920 aaatagaaat ataaatgatt tagttgtttg tttgttaaaa aaaaaaaaaa aaaaaaaaaa 1980 aa 1982 2 537 PRT Momordica charantia 2 Met Ala Val Leu Leu Glu Glu Ile Val Lys Ser Val Glu Leu Trp Leu 1 5 10 15 Arg Leu Ile Lys Lys Pro Gln Pro Tyr Val Asp Pro Asn Leu Asp Pro 20 25 30 Val Leu Leu Ile Pro Gly Val Ala Gly Ser Ile Leu Asn Ala Val Asn 35 40 45 Glu Asp Thr Gly Arg Glu Glu Arg Val Trp Val Arg Ile Leu Gly Ala 50 55 60 Asp Ser Lys Phe Arg Thr Glu Leu Trp Ser Phe Tyr Asp Ser Ala Ser 65 70 75 80 Gly Glu Ser Val Cys Phe Asp Pro Lys Thr Lys Ile Arg Val Pro Asp 85 90 95 Glu Arg Ser Gly Leu Tyr Ala Ile Asp Ile Leu Asp Pro Asp Leu Met 100 105 110 Ile Gly Cys Asp Ser Ile Tyr Tyr Phe His Asp Met Ile Val Glu Met 115 120 125 Thr Lys Trp Gly Phe Gln Glu Gly Lys Thr Leu Phe Gly Phe Gly Tyr 130 135 140 Asp Phe Arg Gln Ser Asn Arg Leu Pro Glu Ser Leu Asp Arg Leu Ala 145 150 155 160 Ala Lys Leu Glu Ala Val Phe Ser Ala Ser Gly Gly Lys Lys Ile Asn 165 170 175 Ile Ile Ser His Ser Met Gly Gly Leu Leu Val Lys Cys Phe Met Cys 180 185 190 Leu Arg Ser Glu Ile Phe Glu Lys Tyr Val Gln Asn Trp Ile Ala Ile 195 200 205 Ala Ala Pro Phe Gln Gly Ala Pro Gly Tyr Val Thr Ser Thr Phe Val 210 215 220 Asn Gly Met Ser Phe Val Asn Gly Trp Lys Gln Asn Phe Phe Ile Ser 225 230 235 240 Lys Trp Ser Met His Gln Leu Leu Ile Glu Cys Pro Ser Ile Tyr Glu 245 250 255 Leu Met Gly Ser Pro Asp Phe Asn Trp Gln His Ile Pro Leu Leu Glu 260 265 270 Ile Trp Arg Gln Lys His Asp Asp Asp Gly Asn Pro His Asn Val Leu 275 280 285 Glu Ser Tyr Leu Leu Lys Glu Ser Val Glu Ile Leu Thr Glu Ser Leu 290 295 300 Ser Thr Asn Ala Ile Leu His Asp Gly Leu Thr Ile Pro Leu Pro Phe 305 310 315 320 Asn Leu Glu Ile Leu Lys Trp Ala Asn Glu Thr Arg Glu Val Leu Lys 325 330 335 Asn Ala Lys Leu Pro Ser Gln Val Lys Phe Tyr Asn Ile Tyr Ala Thr 340 345 350 Gly Leu Glu Thr Pro His Thr Val Cys Tyr Gly Asp Ala Glu Lys Pro 355 360 365 Val Ala Asp Leu His Asn Leu Arg Tyr Ile Glu Pro Asn Tyr Ile Tyr 370 375 380 Val Asp Gly Asp Gly Thr Val Pro Val Glu Ser Ala Lys Ala Asp Gly 385 390 395 400 Leu Asp Ala Val Ala Arg Ile Gly Val Pro Gly Glu His Gln Arg Val 405 410 415 Leu Arg Asp His Arg Val Phe Arg Arg Leu Lys His Trp Leu Lys Ala 420 425 430 Gly Asp Pro Asp Pro Phe Tyr Asp Pro Leu Asn Asp Tyr Val Ile Leu 435 440 445 Pro Thr Ala Phe Glu Val Glu Ser His Val Glu Lys Gly Leu Gln Val 450 455 460 Ala Ala Leu Lys Glu Glu Trp Glu Ile Ile Ser His Asp Gln Asn Lys 465 470 475 480 Thr Asp Glu Leu Cys Asn Asp Lys Pro Leu Val Ser Ser Ile Met Leu 485 490 495 Ser Arg Val Thr Glu Asp Cys Pro Ser Ser Arg Ala Glu Ala Cys Ala 500 505 510 Thr Val Val Val His Pro Gln Gln Asp Gly Lys Gln His Val Glu Leu 515 520 525 Asn Ala Val Ser Val Ser Val Asp Ala 530 535 3 1788 DNA Calendula officinalis 3 gcaccagatt catactttgg gttttaggat ggcggtgttg ctggttgatg tagttaaagc 60 agtagaggca tggttaaaga ttcttaagga accagagcct tacgttgatc cgaatcttga 120 cccggttctt attgttcctg ggattgctgg ttcgattctt catgctaaag atgctgaaac 180 tgggaaagaa gagcgtgttt gggttcggat ctgggaagct gatcgtgagt ttcgtgctaa 240 actttggtgc caatttgatt ctgaaactgg caaaactgtt tctttggatc ccaacatcag 300 catcgttgtc cctgaggaca gaaacgggct ttatgcaatt gattgtttgg atcccaatat 360 gattattggg cgtgatagtg tatgctattt ccatgatatg ataaatgaaa tgacaagttg 420 gggataccaa gaaggaaaaa cgctattcgg ttttggatat gatttccgac aaagcaatag 480 acttaaagaa acaatggatc gtcttgctgc aaaattggat gcaatttata ctgcttcagg 540 agggaaaaag ataactgtaa ttactcattc aatgggtgga cttgttgtca aatgttttat 600 gagtctgcac actgatattt ttgagaaata tgttaagagt tggatagcaa ttgctgcacc 660 atttcagggt gcacctggat atgtaacatc tacattaatg aatgggatgt catttgtgga 720 aggttgggaa gcaaactttt ttgtatccaa gtggagtatg catcaactgc tgattgaatg 780 tccatccata tatgaattaa tggcctgttt ggactatgaa tgggaacatc ttcctctttt 840 acaaatttgg aaagaaattc aggatgaaaa cggtaattct actcccatgc tggagacatt 900 taccccaatg gaatctgttt ccattttcac tcaggccctt tcagtcaatg agttgagctt 960 tgatggagtg gatattcctc taccatttaa caaagaaata ttgcaatggg ctaataaaac 1020 acgagagatc ttatcttcag ccaaacttcc atcaagtgtt aaattctata acgtctatgg 1080 cactggtctt gacactcccc agagtgtatg ttatggaagt gctgattcac ccgtctcaaa 1140 cctattggaa ctaccatttc tagatgcaac ttatgtgaat gttgaaggtg atggaactgt 1200 acctgtagaa tctgccaggg ctgatgggct ggatgcagaa gctagggttg gaatcccagg 1260 tgaacataga ggaattttat gtgacaaaca cctattcagg atagtgaaac actggctaaa 1320 agcagatcat gatccctttt acaatcctgt taacgattat gtaatcctac caactttatt 1380 tgagatcaca aaacatcagg acagcaaaga gggcaaagaa gtaatttcac tcaaagaaga 1440 atgggaaatt gtttcaaaag agcaacaaga tgagcctatg attgggtcaa tttctgcttc 1500 tcgtgttggt gatgatggtt gtgaagaaga agcacgtgca acttttgttg ttcatccaca 1560 aagtaatggt aaacagaata ttcaacttaa tgcggtgagt gtttctgctg gtggtgcgta 1620 aatttgtcat ttgtaattgt ggttgatgaa gttatgtggc gttttctggt aatgtgtata 1680 tatttcagtg tttgtaatga attgaagtga ataaataaaa gaataaagat ggaaaaagaa 1740 gtggttggct tgaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaa 1788 4 530 PRT Calendula officinalis 4 Met Ala Val Leu Leu Val Asp Val Val Lys Ala Val Glu Ala Trp Leu 1 5 10 15 Lys Ile Leu Lys Glu Pro Glu Pro Tyr Val Asp Pro Asn Leu Asp Pro 20 25 30 Val Leu Ile Val Pro Gly Ile Ala Gly Ser Ile Leu His Ala Lys Asp 35 40 45 Ala Glu Thr Gly Lys Glu Glu Arg Val Trp Val Arg Ile Trp Glu Ala 50 55 60 Asp Arg Glu Phe Arg Ala Lys Leu Trp Cys Gln Phe Asp Ser Glu Thr 65 70 75 80 Gly Lys Thr Val Ser Leu Asp Pro Asn Ile Ser Ile Val Val Pro Glu 85 90 95 Asp Arg Asn Gly Leu Tyr Ala Ile Asp Cys Leu Asp Pro Asn Met Ile 100 105 110 Ile Gly Arg Asp Ser Val Cys Tyr Phe His Asp Met Ile Asn Glu Met 115 120 125 Thr Ser Trp Gly Tyr Gln Glu Gly Lys Thr Leu Phe Gly Phe Gly Tyr 130 135 140 Asp Phe Arg Gln Ser Asn Arg Leu Lys Glu Thr Met Asp Arg Leu Ala 145 150 155 160 Ala Lys Leu Asp Ala Ile Tyr Thr Ala Ser Gly Gly Lys Lys Ile Thr 165 170 175 Val Ile Thr His Ser Met Gly Gly Leu Val Val Lys Cys Phe Met Ser 180 185 190 Leu His Thr Asp Ile Phe Glu Lys Tyr Val Lys Ser Trp Ile Ala Ile 195 200 205 Ala Ala Pro Phe Gln Gly Ala Pro Gly Tyr Val Thr Ser Thr Leu Met 210 215 220 Asn Gly Met Ser Phe Val Glu Gly Trp Glu Ala Asn Phe Phe Val Ser 225 230 235 240 Lys Trp Ser Met His Gln Leu Leu Ile Glu Cys Pro Ser Ile Tyr Glu 245 250 255 Leu Met Ala Cys Leu Asp Tyr Glu Trp Glu His Leu Pro Leu Leu Gln 260 265 270 Ile Trp Lys Glu Ile Gln Asp Glu Asn Gly Asn Ser Thr Pro Met Leu 275 280 285 Glu Thr Phe Thr Pro Met Glu Ser Val Ser Ile Phe Thr Gln Ala Leu 290 295 300 Ser Val Asn Glu Leu Ser Phe Asp Gly Val Asp Ile Pro Leu Pro Phe 305 310 315 320 Asn Lys Glu Ile Leu Gln Trp Ala Asn Lys Thr Arg Glu Ile Leu Ser 325 330 335 Ser Ala Lys Leu Pro Ser Ser Val Lys Phe Tyr Asn Val Tyr Gly Thr 340 345 350 Gly Leu Asp Thr Pro Gln Ser Val Cys Tyr Gly Ser Ala Asp Ser Pro 355 360 365 Val Ser Asn Leu Leu Glu Leu Pro Phe Leu Asp Ala Thr Tyr Val Asn 370 375 380 Val Glu Gly Asp Gly Thr Val Pro Val Glu Ser Ala Arg Ala Asp Gly 385 390 395 400 Leu Asp Ala Glu Ala Arg Val Gly Ile Pro Gly Glu His Arg Gly Ile 405 410 415 Leu Cys Asp Lys His Leu Phe Arg Ile Val Lys His Trp Leu Lys Ala 420 425 430 Asp His Asp Pro Phe Tyr Asn Pro Val Asn Asp Tyr Val Ile Leu Pro 435 440 445 Thr Leu Phe Glu Ile Thr Lys His Gln Asp Ser Lys Glu Gly Lys Glu 450 455 460 Val Ile Ser Leu Lys Glu Glu Trp Glu Ile Val Ser Lys Glu Gln Gln 465 470 475 480 Asp Glu Pro Met Ile Gly Ser Ile Ser Ala Ser Arg Val Gly Asp Asp 485 490 495 Gly Cys Glu Glu Glu Ala Arg Ala Thr Phe Val Val His Pro Gln Ser 500 505 510 Asn Gly Lys Gln Asn Ile Gln Leu Asn Ala Val Ser Val Ser Ala Gly 515 520 525 Gly Ala 530 5 2046 DNA Eucalyptus grandis 5 gcaccagaat tcgagcccta attccccacc attctccccc aaatcctcgc cgccgatcgc 60 ctccgtcctt ccgccgctgc cgccgccgat cgccccccgg aaatccgacc tcgaagcgag 120 agtccccccc ggacggacga gcggcgactt ggcggcggag ggcgagattg cgacggcgcc 180 gggaccgggt gtgttagggc tttgattgcg ggcggatggc ggtgctgttg gaggacatcc 240 tgcagtccgt ggagcagtgg ctgaagctga tcaggaagcc ccagccctac gtggacccga 300 acctcgaccc ggtcctcctc gtgcccgggg tcgccggatc gatactgcac gccgtcgacg 360 gcagcaacgg caagggcgag agggtctggg tccggatctt cggggccgac tacaagtgcc 420 ggaccaagct ctggtctcgc ttcgaccctg ccgtcggtaa gaccgtttcc ttagatccta 480 agacgaacat cgtggttcct gaagacagat atggactgta tgccattgat gttttggacc 540 ctgatatggt ccttgggcgt gattgtgtat actatttcca tgacatgata gtcgaaatga 600 tcaaatgggg ttttcaggaa gggaagacat tgttcggttt tgggtatgac ttcaggcaaa 660 gtaacaggtt tcaagaaaca atggagtgtt tggctgcaaa gttggaatct gtatataatg 720 ctgcgggagg gaagaagatg accattatca gtcactctat gggaggtctt ctagtgaagt 780 gctttatgtg cctgcacagt gatatttttg caaagtatgt gaagaattgg attgctatag 840 ctgcaccttt tcaaggtgcc cctggatatg tcacatctac ctttctgaat gggatgtcat 900 ttgtggatgg ttgggagcaa aactttttca tttcaaagtg gagcatgcat cagctgctga 960 ttgaatgccc atcaatctat gaattgatgg catgtccaaa ctttacctgg gaacatgccc 1020 cagtgttaga gatctggagg aagaagcttg atgattgtgg tgatacccgt atgatccttg 1080 agtcttacac cccttccgag agtgtaaata tattcgctga agcactttca agtaatacgg 1140 ttgattatga tggtgagagc atttccttac catttaacca ggaaatcttg aaatgggctc 1200 atgagacccg taggatttta tcttgtgcta aagttccgcc cggggtgaaa ttctacaaca 1260 tatatgcgac caatctggag acaccacaca gtgtttgcta tggcagtgag gacatgcctg 1320 ttacggactt gcaagaactt caattttacc tgcctgatta tatatgtgtt gatggtgatg 1380 gaacagttcc gactgaatca gctaaggcag atgggcttga agcagttgca agagttggag 1440 tacccgggga gcaccgggga attctgtgtg atcatcatgt tttccgcatt ctgaagcact 1500 ggctaaaggc agattcagac ccctactata acccgcttaa cgactatgtg attctaccca 1560 ccacgtttga gatggaaaga caccacgaga agggcatgga ggtgacttca ctcaaagagg 1620 agtgggaaat catttccaaa gatgccaatg atgaccaagg agaggttacc ataatgccct 1680 cagtaagcac cataaccgtt tcccaagaca gaggtcacca atcttatcgg gccgaggctt 1740 gtgccactgt gaccgtgcac ccccaaaatg agggcaagca acaggttgag ctcaatgcct 1800 tgagtgtatc tgttgatgcc taaatttagt tacttgcact gtgtgaaaga aaagcccgca 1860 attggggcag tgctgtgtat agtagtatgt tggtcgtgta caaaatgtgc gtattgtaaa 1920 tataaggatc actggtggca attgccttga tgaaccataa cattggaaga tcgttctggg 1980 ttttgtaatg gaagacccat catctaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa 2040 aaaaaa 2046 6 535 PRT Eucalyptus grandis 6 Met Ala Val Leu Leu Glu Asp Ile Leu Gln Ser Val Glu Gln Trp Leu 1 5 10 15 Lys Leu Ile Arg Lys Pro Gln Pro Tyr Val Asp Pro Asn Leu Asp Pro 20 25 30 Val Leu Leu Val Pro Gly Val Ala Gly Ser Ile Leu His Ala Val Asp 35 40 45 Gly Ser Asn Gly Lys Gly Glu Arg Val Trp Val Arg Ile Phe Gly Ala 50 55 60 Asp Tyr Lys Cys Arg Thr Lys Leu Trp Ser Arg Phe Asp Pro Ala Val 65 70 75 80 Gly Lys Thr Val Ser Leu Asp Pro Lys Thr Asn Ile Val Val Pro Glu 85 90 95 Asp Arg Tyr Gly Leu Tyr Ala Ile Asp Val Leu Asp Pro Asp Met Val 100 105 110 Leu Gly Arg Asp Cys Val Tyr Tyr Phe His Asp Met Ile Val Glu Met 115 120 125 Ile Lys Trp Gly Phe Gln Glu Gly Lys Thr Leu Phe Gly Phe Gly Tyr 130 135 140 Asp Phe Arg Gln Ser Asn Arg Phe Gln Glu Thr Met Glu Cys Leu Ala 145 150 155 160 Ala Lys Leu Glu Ser Val Tyr Asn Ala Ala Gly Gly Lys Lys Met Thr 165 170 175 Ile Ile Ser His Ser Met Gly Gly Leu Leu Val Lys Cys Phe Met Cys 180 185 190 Leu His Ser Asp Ile Phe Ala Lys Tyr Val Lys Asn Trp Ile Ala Ile 195 200 205 Ala Ala Pro Phe Gln Gly Ala Pro Gly Tyr Val Thr Ser Thr Phe Leu 210 215 220 Asn Gly Met Ser Phe Val Asp Gly Trp Glu Gln Asn Phe Phe Ile Ser 225 230 235 240 Lys Trp Ser Met His Gln Leu Leu Ile Glu Cys Pro Ser Ile Tyr Glu 245 250 255 Leu Met Ala Cys Pro Asn Phe Thr Trp Glu His Ala Pro Val Leu Glu 260 265 270 Ile Trp Arg Lys Lys Leu Asp Asp Cys Gly Asp Thr Arg Met Ile Leu 275 280 285 Glu Ser Tyr Thr Pro Ser Glu Ser Val Asn Ile Phe Ala Glu Ala Leu 290 295 300 Ser Ser Asn Thr Val Asp Tyr Asp Gly Glu Ser Ile Ser Leu Pro Phe 305 310 315 320 Asn Gln Glu Ile Leu Lys Trp Ala His Glu Thr Arg Arg Ile Leu Ser 325 330 335 Cys Ala Lys Val Pro Pro Gly Val Lys Phe Tyr Asn Ile Tyr Ala Thr 340 345 350 Asn Leu Glu Thr Pro His Ser Val Cys Tyr Gly Ser Glu Asp Met Pro 355 360 365 Val Thr Asp Leu Gln Glu Leu Gln Phe Tyr Leu Pro Asp Tyr Ile Cys 370 375 380 Val Asp Gly Asp Gly Thr Val Pro Thr Glu Ser Ala Lys Ala Asp Gly 385 390 395 400 Leu Glu Ala Val Ala Arg Val Gly Val Pro Gly Glu His Arg Gly Ile 405 410 415 Leu Cys Asp His His Val Phe Arg Ile Leu Lys His Trp Leu Lys Ala 420 425 430 Asp Ser Asp Pro Tyr Tyr Asn Pro Leu Asn Asp Tyr Val Ile Leu Pro 435 440 445 Thr Thr Phe Glu Met Glu Arg His His Glu Lys Gly Met Glu Val Thr 450 455 460 Ser Leu Lys Glu Glu Trp Glu Ile Ile Ser Lys Asp Ala Asn Asp Asp 465 470 475 480 Gln Gly Glu Val Thr Ile Met Pro Ser Val Ser Thr Ile Thr Val Ser 485 490 495 Gln Asp Arg Gly His Gln Ser Tyr Arg Ala Glu Ala Cys Ala Thr Val 500 505 510 Thr Val His Pro Gln Asn Glu Gly Lys Gln Gln Val Glu Leu Asn Ala 515 520 525 Leu Ser Val Ser Val Asp Ala 530 535 7 2043 DNA Vitis sp. 7 gcttctctct ccaattaaca actcgtctcc aaaccccaat ttcatccgat tttcatctca 60 aattcatctc tagttttcga tcgttgtgtc tggtggtcgc caagtttgaa tccgcttgcg 120 gctaaagttt ctcagaattt ggaatcggag ggataggtta gatgcatttg tcggaattga 180 gttgcgatta gggtttcgga gatggcggtg ttgttggagg agatagcgca gtcggtggag 240 atatggttga agctgattaa gaaacctcag ccgtacgttg accccaatct tgacccggtt 300 ctgttggtgc ccggcatcgc cggttcgatc ctgaaagccg tcgacgacaa tggtcgcggc 360 gagcgggttt gggtccggat aatcggtgcc gattacaagt tccggactaa gctttggtcg 420 cgatttgacc cctctactgg tcaaacagtg tctttagatc caaaaaccca tattgtggtc 480 cctgaagaga gatatggatt gcatgcaatt gatgtcttgg atcctgaaat gattattggg 540 cgtgattgtg tttattattt ccatgacatg atagttgaaa tgatgaaatg gggttttcaa 600 gagggaaaaa cactatttgg ttttggttat gatttccgcc aaagtaacag gtttcaggaa 660 acactagagc gctttgctgc gaaactggag gctgtgtaca ccgcctcagg aggaaaaaaa 720 ataaacataa taagtcattc tatggggggt ctacttgtga aatgtttcat gagtttacac 780 actgatatct ttgagaagta tgtgcagaac tggatagcaa ttgctgcacc attccagggt 840 gcacctggat atatctcatc gacatttctg aatggaatgt catttgtgga aggttgggaa 900 cagaattttt ttatatcaaa atggagcatg caccagctgc ttattgaatg tccatcaata 960 tatgaattga tggcttgtcc ggattttcaa tgggaacaca atccactttt ggaaatttgg 1020 agagagaagc atgataagga tggtaactct aacattgttc tggagtctta ttccccagaa 1080 gaaagtgttc caatttttaa ggaagctctt tccagtaata cggttaatta cgatggattg 1140 gacattcctc tacctttcaa tttagagatc ttgcaatggg cttgtgaaac acgcaagatc 1200 ttatcttgtg ctaaggttcc ttctcaagtt aaattttaca atatatatgg gatgaacctc 1260 gagacgcctc atagtgtttg ttatggaagt gtggaagaac ctgttacaga tctagagcaa 1320 ttaaaatttg tccaggctca atatgtatgc gttgatggtg atgggactgt tccagtggaa 1380 tcagcaatgg cggatgggct tactgcagaa gcaaggattg gagtccctgg tgagcaccgg 1440 ggaatccttg ctgaaccgca tgtatttcgg attctaaaac actggctgaa ggcaggggac 1500 ccagatcctt actacaatcc tctaaacgat tacgtgatcc tgcccactgc atttgaaatg 1560 gagaggcaca aagagagagg cctgcaggtg acttccctca aagaagaatg ggaaatcatc 1620 tctagagact caaacgatga ggacaatatc atcgtcaaca acgggaagcc tctggtaagc 1680 tcaatagctg tttctgatca gtcatctctg acagaggctc gagccaccgt cactcttcac 1740 ccccagagtg agggcaagcg acacattgaa ctaaatgcca taagcgtttc tgcaactgtt 1800 taaaacccag ttggtggtga aaaattgtca tcagctctgg gattcaatgg tctctactgt 1860 atagttgcta ttccttcagt ttgaactttg aagccggtat cccttgtgcc tcttgtgtgt 1920 atatagtgtt cctggaagaa gggtttcatg taagatctat tctggacaaa ttcattcatg 1980 ggatatatga atatatgcat atatacatat atataatatt tgttaaaaaa aaaaaaaaaa 2040 aaa 2043 8 533 PRT Vitis sp. 8 Met Ala Val Leu Leu Glu Glu Ile Ala Gln Ser Val Glu Ile Trp Leu 1 5 10 15 Lys Leu Ile Lys Lys Pro Gln Pro Tyr Val Asp Pro Asn Leu Asp Pro 20 25 30 Val Leu Leu Val Pro Gly Ile Ala Gly Ser Ile Leu Lys Ala Val Asp 35 40 45 Asp Asn Gly Arg Gly Glu Arg Val Trp Val Arg Ile Ile Gly Ala Asp 50 55 60 Tyr Lys Phe Arg Thr Lys Leu Trp Ser Arg Phe Asp Pro Ser Thr Gly 65 70 75 80 Gln Thr Val Ser Leu Asp Pro Lys Thr His Ile Val Val Pro Glu Glu 85 90 95 Arg Tyr Gly Leu His Ala Ile Asp Val Leu Asp Pro Glu Met Ile Ile 100 105 110 Gly Arg Asp Cys Val Tyr Tyr Phe His Asp Met Ile Val Glu Met Met 115 120 125 Lys Trp Gly Phe Gln Glu Gly Lys Thr Leu Phe Gly Phe Gly Tyr Asp 130 135 140 Phe Arg Gln Ser Asn Arg Phe Gln Glu Thr Leu Glu Arg Phe Ala Ala 145 150 155 160 Lys Leu Glu Ala Val Tyr Thr Ala Ser Gly Gly Lys Lys Ile Asn Ile 165 170 175 Ile Ser His Ser Met Gly Gly Leu Leu Val Lys Cys Phe Met Ser Leu 180 185 190 His Thr Asp Ile Phe Glu Lys Tyr Val Gln Asn Trp Ile Ala Ile Ala 195 200 205 Ala Pro Phe Gln Gly Ala Pro Gly Tyr Ile Ser Ser Thr Phe Leu Asn 210 215 220 Gly Met Ser Phe Val Glu Gly Trp Glu Gln Asn Phe Phe Ile Ser Lys 225 230 235 240 Trp Ser Met His Gln Leu Leu Ile Glu Cys Pro Ser Ile Tyr Glu Leu 245 250 255 Met Ala Cys Pro Asp Phe Gln Trp Glu His Asn Pro Leu Leu Glu Ile 260 265 270 Trp Arg Glu Lys His Asp Lys Asp Gly Asn Ser Asn Ile Val Leu Glu 275 280 285 Ser Tyr Ser Pro Glu Glu Ser Val Pro Ile Phe Lys Glu Ala Leu Ser 290 295 300 Ser Asn Thr Val Asn Tyr Asp Gly Leu Asp Ile Pro Leu Pro Phe Asn 305 310 315 320 Leu Glu Ile Leu Gln Trp Ala Cys Glu Thr Arg Lys Ile Leu Ser Cys 325 330 335 Ala Lys Val Pro Ser Gln Val Lys Phe Tyr Asn Ile Tyr Gly Met Asn 340 345 350 Leu Glu Thr Pro His Ser Val Cys Tyr Gly Ser Val Glu Glu Pro Val 355 360 365 Thr Asp Leu Glu Gln Leu Lys Phe Val Gln Ala Gln Tyr Val Cys Val 370 375 380 Asp Gly Asp Gly Thr Val Pro Val Glu Ser Ala Met Ala Asp Gly Leu 385 390 395 400 Thr Ala Glu Ala Arg Ile Gly Val Pro Gly Glu His Arg Gly Ile Leu 405 410 415 Ala Glu Pro His Val Phe Arg Ile Leu Lys His Trp Leu Lys Ala Gly 420 425 430 Asp Pro Asp Pro Tyr Tyr Asn Pro Leu Asn Asp Tyr Val Ile Leu Pro 435 440 445 Thr Ala Phe Glu Met Glu Arg His Lys Glu Arg Gly Leu Gln Val Thr 450 455 460 Ser Leu Lys Glu Glu Trp Glu Ile Ile Ser Arg Asp Ser Asn Asp Glu 465 470 475 480 Asp Asn Ile Ile Val Asn Asn Gly Lys Pro Leu Val Ser Ser Ile Ala 485 490 495 Val Ser Asp Gln Ser Ser Leu Thr Glu Ala Arg Ala Thr Val Thr Leu 500 505 510 His Pro Gln Ser Glu Gly Lys Arg His Ile Glu Leu Asn Ala Ile Ser 515 520 525 Val Ser Ala Thr Val 530 9 1438 DNA Oryza sativa 9 tctctctctc ggaaaacatt atttggattt ggttatgatt tccgccagag taacaggctt 60 tcagaaacac ttgatagatt ttccagaaag ttggagtcag tttacatagc ttccggagaa 120 aaaaagatca atctcattac tcattcaatg ggaggattgc ttgtcaaatg cttcatgtcc 180 ctccatagtg atgtcttcga gaaatacata aagagttgga ttgcaattgc tgcaccattt 240 caaggtgcac ctgggtacat aactactagt ctgctgaatg gtatgtcttt tgtcgaagga 300 tgggagtcaa gattctttat ttccaagtgg agtatgcagc aattgttgct cgaatgccca 360 tcaatttacg aattgttggc taactcgacc ttccaatggg aagatactcc atatctgcag 420 atctggagac agaaattgga tactaatggc aagaaaagtg ccatgttaga gtcatatgag 480 ccagatgaag caataaaaat gattagagaa gctctttcca agcatgagat catttctgat 540 ggtatgcaca ttccattgcc ccttgatatg gatatattga gatgggcaaa agagacacag 600 gatgttttgt gcaatgcaaa gcttccaaaa tcagtgaagt tctacaatat ttacggaact 660 gattatgaca ctgcccatac cgttcgctac gggagtgaac accatccaat ttcaaatctc 720 agtgacctct tgtatactca gtcaggcaac tacatctgtg ttgatggtga tggatctgtc 780 cctgtagaat cagcaaaggc agatggcctc gatgcagtgg caagagttgg ggttgctgca 840 gaccaccgag gaatcgtctg tgatcgtcac gtgttccgga taattcagca ctggctccat 900 gccggtgagc ctgacccatt ctacgatccc ctcaacgact acgtcatact cccaacagcc 960 ttcgagatcg agaagtacca cgagaaacac ggggatatca catcggttag agaggactgg 1020 gagatcatct cccatcgcga tgacgaaagc aagaggccag ccgagcttcc tcctatgttc 1080 aacacgctat cggcgtcccg cgagggtgaa gacggctcgc tggaagaggc gcaggcgacg 1140 atctttgttc atccagagag caaagggagg cagcatgtgg aagttagggc agttggagtc 1200 acccatgacg gctagtcaag ccagtcatac gaaaacacac ggttgtcaac tagctagtct 1260 gcacactcca aagcaaagtg gacaatgtaa atataagacg tccctagcta tgaactacgt 1320 gtaattttgc tgccttgtaa ataccagaac tgaaaatata ctgccactgg atgatgatac 1380 gaatagaaag gagaaagaaa aggatgaact tgatatgtta aaaaaaaaaa aaaaaaaa 1438 10 404 PRT Oryza sativa 10 Ser Leu Ser Arg Lys Thr Leu Phe Gly Phe Gly Tyr Asp Phe Arg Gln 1 5 10 15 Ser Asn Arg Leu Ser Glu Thr Leu Asp Arg Phe Ser Arg Lys Leu Glu 20 25 30 Ser Val Tyr Ile Ala Ser Gly Glu Lys Lys Ile Asn Leu Ile Thr His 35 40 45 Ser Met Gly Gly Leu Leu Val Lys Cys Phe Met Ser Leu His Ser Asp 50 55 60 Val Phe Glu Lys Tyr Ile Lys Ser Trp Ile Ala Ile Ala Ala Pro Phe 65 70 75 80 Gln Gly Ala Pro Gly Tyr Ile Thr Thr Ser Leu Leu Asn Gly Met Ser 85 90 95 Phe Val Glu Gly Trp Glu Ser Arg Phe Phe Ile Ser Lys Trp Ser Met 100 105 110 Gln Gln Leu Leu Leu Glu Cys Pro Ser Ile Tyr Glu Leu Leu Ala Asn 115 120 125 Ser Thr Phe Gln Trp Glu Asp Thr Pro Tyr Leu Gln Ile Trp Arg Gln 130 135 140 Lys Leu Asp Thr Asn Gly Lys Lys Ser Ala Met Leu Glu Ser Tyr Glu 145 150 155 160 Pro Asp Glu Ala Ile Lys Met Ile Arg Glu Ala Leu Ser Lys His Glu 165 170 175 Ile Ile Ser Asp Gly Met His Ile Pro Leu Pro Leu Asp Met Asp Ile 180 185 190 Leu Arg Trp Ala Lys Glu Thr Gln Asp Val Leu Cys Asn Ala Lys Leu 195 200 205 Pro Lys Ser Val Lys Phe Tyr Asn Ile Tyr Gly Thr Asp Tyr Asp Thr 210 215 220 Ala His Thr Val Arg Tyr Gly Ser Glu His His Pro Ile Ser Asn Leu 225 230 235 240 Ser Asp Leu Leu Tyr Thr Gln Ser Gly Asn Tyr Ile Cys Val Asp Gly 245 250 255 Asp Gly Ser Val Pro Val Glu Ser Ala Lys Ala Asp Gly Leu Asp Ala 260 265 270 Val Ala Arg Val Gly Val Ala Ala Asp His Arg Gly Ile Val Cys Asp 275 280 285 Arg His Val Phe Arg Ile Ile Gln His Trp Leu His Ala Gly Glu Pro 290 295 300 Asp Pro Phe Tyr Asp Pro Leu Asn Asp Tyr Val Ile Leu Pro Thr Ala 305 310 315 320 Phe Glu Ile Glu Lys Tyr His Glu Lys His Gly Asp Ile Thr Ser Val 325 330 335 Arg Glu Asp Trp Glu Ile Ile Ser His Arg Asp Asp Glu Ser Lys Arg 340 345 350 Pro Ala Glu Leu Pro Pro Met Phe Asn Thr Leu Ser Ala Ser Arg Glu 355 360 365 Gly Glu Asp Gly Ser Leu Glu Glu Ala Gln Ala Thr Ile Phe Val His 370 375 380 Pro Glu Ser Lys Gly Arg Gln His Val Glu Val Arg Ala Val Gly Val 385 390 395 400 Thr His Asp Gly 11 1475 DNA Vernonia mespilifolia unsure (1471) n = a, c, g or t 11 aatcgattgc ttggatcctg atatgctcat tgggcgtgat agtgtatgct acttccatga 60 aatgataaat gaaatgacaa gctggggata cctagaagga aaaacgcttt ttgggtttgg 120 gtatgatttc cgacaaagca acagacttca agaaactatg gatcgtcttg ctacaaagtt 180 ggaatctatc tatacttctt caggggggaa aaaaataaat gtaattactc attcaatggg 240 cggacttctt gtcaaatgtt ttatgagcct gcacagtgat atttttgaga aatatgttaa 300 gaattggata gcaattgytg caccatttca gggtgctcct ggatatgtaa catytacatt 360 attgaatggg atgtcatttg tggaagggtg ggaagcatac tttttsrtat ccmagtggar 420 tatgcatcag ctgctgattg aatgtccatc catctatgaa ttgatggcct gtctggacta 480 tgaatgggaa catgatccat tgttacaaat ttggaaggag attcagaatg atgatggaaa 540 ctctaccact attctggaga cattcacccc agtggaagct gtttcgatct tcactcaggc 600 tctgtcaatc aacgagctga actatggtgg agtggatatc cctctaccat tcaacaaaga 660 aatattgcat tgggctaaca aaacacgaga gatcttgtct tcagccaaac ttccaccaaa 720 tgttaaattc tataatgtat atggcactgg tcgtgacact cctcagagtg tatgttacgg 780 aagcgcagac tcacccgtct cggacctaca ggaattaccg ttgctcgatg ctactttcat 840 caatgttgat ggtgatggga ccgtacccat ggaatctgca aaggctgatg ggctagacgc 900 agaagctagg gttggtatcc caggtgaaca ccgagggatc ttattagaca agcatttgtt 960 ccggatagtc aagcattggc tgaaggcaga tcacgatccc ttctacaacc ctgtgaatga 1020 ttatgtgatc ctaccgacta tattcgagat cgagcggcac aaggaaaagg gcttagaagt 1080 aatgtcactc aaggaagaat gggaactcgt ttccggagac caagaagatg atgacaccta 1140 cgacaataga aaaccaatgg ttggatcgat atcagcttct catgtaggag acgatggatc 1200 ttttgatgaa gtggcacgtg cgactttcat cgttcatccg cagagcaacg gcaaacaaca 1260 tattgaattg aatgccatga gtgttactgc tggtggtgca taattctggt ggttaatgaa 1320 tttatcattc tgtttatgta tatattgttc aagtgtttgt ttaaatgagt ttaaataaaa 1380 ttttaataaa aaaatatgat ggaaacaact cgwtktgtak cccggtaccc aattcgccct 1440 atagtgagtc gtattacaat tcactggccg nccgg 1475 12 433 PRT Vernonia mespilifolia UNSURE (106) Xaa = any amino acid 12 Ile Asp Cys Leu Asp Pro Asp Met Leu Ile Gly Arg Asp Ser Val Cys 1 5 10 15 Tyr Phe His Glu Met Ile Asn Glu Met Thr Ser Trp Gly Tyr Leu Glu 20 25 30 Gly Lys Thr Leu Phe Gly Phe Gly Tyr Asp Phe Arg Gln Ser Asn Arg 35 40 45 Leu Gln Glu Thr Met Asp Arg Leu Ala Thr Lys Leu Glu Ser Ile Tyr 50 55 60 Thr Ser Ser Gly Gly Lys Lys Ile Asn Val Ile Thr His Ser Met Gly 65 70 75 80 Gly Leu Leu Val Lys Cys Phe Met Ser Leu His Ser Asp Ile Phe Glu 85 90 95 Lys Tyr Val Lys Asn Trp Ile Ala Ile Xaa Ala Pro Phe Gln Gly Ala 100 105 110 Pro Gly Tyr Val Thr Xaa Thr Leu Leu Asn Gly Met Ser Phe Val Glu 115 120 125 Gly Trp Glu Ala Tyr Phe Xaa Xaa Ser Xaa Trp Xaa Met His Gln Leu 130 135 140 Leu Ile Glu Cys Pro Ser Ile Tyr Glu Leu Met Ala Cys Leu Asp Tyr 145 150 155 160 Glu Trp Glu His Asp Pro Leu Leu Gln Ile Trp Lys Glu Ile Gln Asn 165 170 175 Asp Asp Gly Asn Ser Thr Thr Ile Leu Glu Thr Phe Thr Pro Val Glu 180 185 190 Ala Val Ser Ile Phe Thr Gln Ala Leu Ser Ile Asn Glu Leu Asn Tyr 195 200 205 Gly Gly Val Asp Ile Pro Leu Pro Phe Asn Lys Glu Ile Leu His Trp 210 215 220 Ala Asn Lys Thr Arg Glu Ile Leu Ser Ser Ala Lys Leu Pro Pro Asn 225 230 235 240 Val Lys Phe Tyr Asn Val Tyr Gly Thr Gly Arg Asp Thr Pro Gln Ser 245 250 255 Val Cys Tyr Gly Ser Ala Asp Ser Pro Val Ser Asp Leu Gln Glu Leu 260 265 270 Pro Leu Leu Asp Ala Thr Phe Ile Asn Val Asp Gly Asp Gly Thr Val 275 280 285 Pro Met Glu Ser Ala Lys Ala Asp Gly Leu Asp Ala Glu Ala Arg Val 290 295 300 Gly Ile Pro Gly Glu His Arg Gly Ile Leu Leu Asp Lys His Leu Phe 305 310 315 320 Arg Ile Val Lys His Trp Leu Lys Ala Asp His Asp Pro Phe Tyr Asn 325 330 335 Pro Val Asn Asp Tyr Val Ile Leu Pro Thr Ile Phe Glu Ile Glu Arg 340 345 350 His Lys Glu Lys Gly Leu Glu Val Met Ser Leu Lys Glu Glu Trp Glu 355 360 365 Leu Val Ser Gly Asp Gln Glu Asp Asp Asp Thr Tyr Asp Asn Arg Lys 370 375 380 Pro Met Val Gly Ser Ile Ser Ala Ser His Val Gly Asp Asp Gly Ser 385 390 395 400 Phe Asp Glu Val Ala Arg Ala Thr Phe Ile Val His Pro Gln Ser Asn 405 410 415 Gly Lys Gln His Ile Glu Leu Asn Ala Met Ser Val Thr Ala Gly Gly 420 425 430 Ala 13 634 DNA Triticum aestivum 13 cgcctccgga atccccaccc ccgtccaaat ccgggcaaac catatacccc agctacccgc 60 cgcggagcag attccccgcc atccgccgac gccacgccac gccacccccg tgccgctccg 120 attcgagctt gccggagctc ggtttggccg gaagcctcgc cctctcatgc tgatctcgcg 180 gccgggggct tgagagtgct tatttagggc ggggatttgg gcggcgggga agcaaggatg 240 tcggtgctgg aggatttgat ccgggcgatc gagctgtggc tgcggatcgc caaggagcag 300 gtgccgctgg tcgaccccag cctcgacccg gtgctgctcg tgcccggcat cggcggctcc 360 atcctcgagg ccgtggacga ggccgggaac aaggagcggg tctgggtgcg catcctcgcc 420 gccgaccacg agtgccgcga gaagctctgg gcgcagttcg atgcctccac tggcaaaact 480 atttctgtgg atgagaaaat acgcatcact gtcccggagg ataggtatgg attgtacgcc 540 atcgacacat tggacccaga cctgattatt ggtgatgaca gtgtttacta ctatcatgac 600 atgatagtgc aaatgattaa atggggatat caag 634 14 132 PRT Triticum aestivum 14 Met Ser Val Leu Glu Asp Leu Ile Arg Ala Ile Glu Leu Trp Leu Arg 1 5 10 15 Ile Ala Lys Glu Gln Val Pro Leu Val Asp Pro Ser Leu Asp Pro Val 20 25 30 Leu Leu Val Pro Gly Ile Gly Gly Ser Ile Leu Glu Ala Val Asp Glu 35 40 45 Ala Gly Asn Lys Glu Arg Val Trp Val Arg Ile Leu Ala Ala Asp His 50 55 60 Glu Cys Arg Glu Lys Leu Trp Ala Gln Phe Asp Ala Ser Thr Gly Lys 65 70 75 80 Thr Ile Ser Val Asp Glu Lys Ile Arg Ile Thr Val Pro Glu Asp Arg 85 90 95 Tyr Gly Leu Tyr Ala Ile Asp Thr Leu Asp Pro Asp Leu Ile Ile Gly 100 105 110 Asp Asp Ser Val Tyr Tyr Tyr His Asp Met Ile Val Gln Met Ile Lys 115 120 125 Trp Gly Tyr Gln 130 15 1510 DNA C. tetragonoloba 15 gcacgagggc atatcaaagc agtgatgaac attgggggac catttcttgg tgttccaaaa 60 tcagttgctg gacttttctc tctagaggcc agggatatcg ctgttgccag ggcattcgca 120 ccaggagttt tggataaaga tgtttttggt cttcaaactt tactgcatct aatgcggatg 180 acccgaacat gggattcaac tatgtcaatg ataccaaaag gtggggatac tatatggggt 240 ggccttgatt ggtcacctga aggacactat agctgcagtg caaagaagct caagaaaaat 300 gatacttaca attcatttca aaatgacaaa gagaatctta agttcgtgaa aagtgtgaac 360 tatgggagac tcatatcatt tgggaaacat atcgctgagt tacattcttc caagcttgag 420 aggttggatt ttaggggtgc tcttaagggt aggaaccttg caaacacatc tagttgtgat 480 gtctggacag agtaccatga aatgggtatt gaaggaatca aagctgttct agattacaaa 540 acttacacag ctgactcagt cttggatttg cttcattatg ttgctcccaa gatgatgaag 600 cgtggagatg ctcatttttc tcatgggatt gctgataatt tggatgatga gaaataccaa 660 cattacaagt actggtctaa ccccttagaa acaaggttac caaatgctcc agatatggaa 720 atttactcta tgtacggggt tgggatccct acagaaagag cctatgtcta caaatttaat 780 cctcaatctg aatgccaaat cccctttcag attgacacat cagctgatgg cgaaaatgag 840 gactcatgtc taaaggatgg agtttattgt tctgatggtg atgaaactgt tcctgtttta 900 agtgctggtt tcatgtgtgc aaagggttgg cggggaaaaa cccgcttcaa tccttccgga 960 attcatacat acataaggga gtatgatcat gcccctccag ctaatcttct agaaggccgg 1020 ggaacccaga gtggtgctca tgttgatata ttgggtaact ttgcattgat tgaagatatt 1080 atacgagtag cggctggagc ctccggtgaa gacctgggtg gtgatcgagt gtactctgat 1140 attttcaaat ggtctgaaaa tatcaatttg aagctctaga ttcacatgta cgagatcaaa 1200 tcccatctcc ttcaaaccat cttgccagag attgacctaa tggtatgaac tacaaagctg 1260 atgcattgtt gacagcggca acttgcttta tgctaggatt ttatctgtag gaaagaaatt 1320 acacaatatc ttagttgtag gaacatgttt cagattttgt ttattctatt catttgtttg 1380 gattattgtc aggtattagt gtcaagtgtc caatactaac tattcgtgag acctgttata 1440 gaccagttag tggaaaatag gacataattt aatagataat gcgcttcaaa ttaaaaaaaa 1500 aaaaaaaaaa 1510 16 389 PRT C. tetragonoloba 16 His Ile Lys Ala Val Met Asn Ile Gly Gly Pro Phe Leu Gly Val Pro 1 5 10 15 Lys Ser Val Ala Gly Leu Phe Ser Leu Glu Ala Arg Asp Ile Ala Val 20 25 30 Ala Arg Ala Phe Ala Pro Gly Val Leu Asp Lys Asp Val Phe Gly Leu 35 40 45 Gln Thr Leu Leu His Leu Met Arg Met Thr Arg Thr Trp Asp Ser Thr 50 55 60 Met Ser Met Ile Pro Lys Gly Gly Asp Thr Ile Trp Gly Gly Leu Asp 65 70 75 80 Trp Ser Pro Glu Gly His Tyr Ser Cys Ser Ala Lys Lys Leu Lys Lys 85 90 95 Asn Asp Thr Tyr Asn Ser Phe Gln Asn Asp Lys Glu Asn Leu Lys Phe 100 105 110 Val Lys Ser Val Asn Tyr Gly Arg Leu Ile Ser Phe Gly Lys His Ile 115 120 125 Ala Glu Leu His Ser Ser Lys Leu Glu Arg Leu Asp Phe Arg Gly Ala 130 135 140 Leu Lys Gly Arg Asn Leu Ala Asn Thr Ser Ser Cys Asp Val Trp Thr 145 150 155 160 Glu Tyr His Glu Met Gly Ile Glu Gly Ile Lys Ala Val Leu Asp Tyr 165 170 175 Lys Thr Tyr Thr Ala Asp Ser Val Leu Asp Leu Leu His Tyr Val Ala 180 185 190 Pro Lys Met Met Lys Arg Gly Asp Ala His Phe Ser His Gly Ile Ala 195 200 205 Asp Asn Leu Asp Asp Glu Lys Tyr Gln His Tyr Lys Tyr Trp Ser Asn 210 215 220 Pro Leu Glu Thr Arg Leu Pro Asn Ala Pro Asp Met Glu Ile Tyr Ser 225 230 235 240 Met Tyr Gly Val Gly Ile Pro Thr Glu Arg Ala Tyr Val Tyr Lys Phe 245 250 255 Asn Pro Gln Ser Glu Cys Gln Ile Pro Phe Gln Ile Asp Thr Ser Ala 260 265 270 Asp Gly Glu Asn Glu Asp Ser Cys Leu Lys Asp Gly Val Tyr Cys Ser 275 280 285 Asp Gly Asp Glu Thr Val Pro Val Leu Ser Ala Gly Phe Met Cys Ala 290 295 300 Lys Gly Trp Arg Gly Lys Thr Arg Phe Asn Pro Ser Gly Ile His Thr 305 310 315 320 Tyr Ile Arg Glu Tyr Asp His Ala Pro Pro Ala Asn Leu Leu Glu Gly 325 330 335 Arg Gly Thr Gln Ser Gly Ala His Val Asp Ile Leu Gly Asn Phe Ala 340 345 350 Leu Ile Glu Asp Ile Ile Arg Val Ala Ala Gly Ala Ser Gly Glu Asp 355 360 365 Leu Gly Gly Asp Arg Val Tyr Ser Asp Ile Phe Lys Trp Ser Glu Asn 370 375 380 Ile Asn Leu Lys Leu 385 17 2479 DNA Parthenium argentatum Grey 17 gcaccagctc cgccggttgc atacgtcatc atcacgtaat gtcactactt cgaagaagaa 60 agcaaccaca acaccatccg gatccaacac cagacgaaga aaacgaagaa aaggaacaaa 120 aagcgtttaa aaaacaagca aaaaccaaca aaacaaaaaa ctacacgtgt ctggataact 180 gctgttggtt cgtgggatgc gtatgttcag tatggtggtt attattattt ttatacaacg 240 cgatgccagc gtcgttccct cagtttgtaa cggaggctat atccggaccg gttccggatc 300 ctccaggggt taagtgtttg aaagaagggt tgaaggcgaa gcatccggtg gtgtttgtgc 360 ccgggattgt gaccggtggg cttgagctgt gggaagggca tcagtgtatg gatgggttgt 420 ttaggaagag gctgtggggt ggtacgtttg gtgaggttta taaaaggcct tcatgttggg 480 tacaacatat gtccctggac aacaaaactg ggatggatcc gccaggtata cgggtcagac 540 ccgttagtgg acttgtagct gctgactact ttgccccggg atattttgtt tgggctgttt 600 tgattgctaa cttggcgcgt gttggatatg aagagaaaaa tatgtatatg gctgcatatg 660 actggagact ctcgtttcaa aacacggagg taagagacca aacattgagt cggataaaga 720 gcaatataga actgatggtt gctacaaatg gtgggaaaaa ggcggttatt atcccacatt 780 caatgggtgt tatctacttc ctgcatttca tgaaatgggt cgaagcacca gctccaatgg 840 gtggtggagg tggaccagat tggtgtgcta aacatatcaa agcggtaatg aacattggtg 900 gaccattttt aggtgtccca aaagctgtag ccgggctttt ctctgcagaa gctaaagata 960 ttgcatcagt cagggctctt gcaccaggta tgttggactc ggatttattt cagattcaga 1020 cgttacaaca tataatgaga atgagccgca catgggattc aaccatgtct atgataccaa 1080 aaggcgggga caccatttgg ggcggtcttg attggtctcc cgaagacggg tatagtccaa 1140 gtaagagaaa acatggaaaa aatgacactg aatcttctac ccaaaatgag tctgcaagtg 1200 aagaatgtga agtaacacac gcaaattatg gaaggatagt atcatttggg agagatgtag 1260 cagaggcacc atcttcagag atcgagagga tagaatttag gggtgctgtg aagggtaaca 1320 atgttgcaaa caatacatgc cgggccgtgt ggaccgaata ccatgacatg ggatttggtg 1380 gaatcaaggc tgttgcagag tacaaggtat atacagctgg cgaaattgtg gatatgctgg 1440 agtttgttgc tccaaaaatg atggaacgcg gcagtgctca tttttcatat ggtatagctg 1500 acaatttgga tgacccaaaa tactcacatt acaagtattg gtctaaccca ttagagacaa 1560 agctaccaaa cgctccagac atggagatct attcaatgta tggagttggc atcccaactg 1620 aaagagcata tgtttataaa ctcacacctg cagcagaatg ctacatacca ttccaaattg 1680 acacgtcggc aaaagataaa aacgaggatg ggtgtttaaa agatggagtt tatacggttg 1740 acggagatga aacagtacca gcattaagcg caggctacat gtgtgcaaaa ggttggcgtg 1800 ggaaaactag attcaatcct tcgggaatca aaacgtatgt tagggaatac gatcacaatc 1860 ctccatccaa ctttcttgag ggccggggca cgcaaagcgg ggctcacgtg gatattatgg 1920 gtaatttcca gttaattgaa gatgttataa aggttgcagc cggagccacg ggtgaagaac 1980 tgggaggtga tcaggtgtac acaggtatat tcgagtggtc cgagaaaatc aatttagagt 2040 tatgaaatat ttgaggtagg aattatacaa acaatatatt ggggtgcgtt tattgcataa 2100 tcagttttga ttagagaatt gcgagaacct aagtactttg taccggtgca tggaagatgt 2160 gatagcgtct tttgtatcat acttaaagca ataagtattc gggttagtgt acttctcgca 2220 gttctgtatt tgattttggc tctgtattaa acgtaactcc gtgtgcatta ttgatccaca 2280 aatctgtact gtgggtggat tattttgtaa tttgtagcat gttgcttcct taaacagcca 2340 taaaaatttg tttgttgtat cttgatatat gtaatcattt ttaggaagga gttaacattt 2400 atatgtaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa 2460 aaaaaaaaaa aaaaaaaaa 2479 18 668 PRT Parthenium argentatum Grey 18 Met Ser Leu Leu Arg Arg Arg Lys Gln Pro Gln His His Pro Asp Pro 1 5 10 15 Thr Pro Asp Glu Glu Asn Glu Glu Lys Glu Gln Lys Ala Phe Lys Lys 20 25 30 Gln Ala Lys Thr Asn Lys Thr Lys Asn Tyr Thr Cys Leu Asp Asn Cys 35 40 45 Cys Trp Phe Val Gly Cys Val Cys Ser Val Trp Trp Leu Leu Leu Phe 50 55 60 Leu Tyr Asn Ala Met Pro Ala Ser Phe Pro Gln Phe Val Thr Glu Ala 65 70 75 80 Ile Ser Gly Pro Val Pro Asp Pro Pro Gly Val Lys Cys Leu Lys Glu 85 90 95 Gly Leu Lys Ala Lys His Pro Val Val Phe Val Pro Gly Ile Val Thr 100 105 110 Gly Gly Leu Glu Leu Trp Glu Gly His Gln Cys Met Asp Gly Leu Phe 115 120 125 Arg Lys Arg Leu Trp Gly Gly Thr Phe Gly Glu Val Tyr Lys Arg Pro 130 135 140 Ser Cys Trp Val Gln His Met Ser Leu Asp Asn Lys Thr Gly Met Asp 145 150 155 160 Pro Pro Gly Ile Arg Val Arg Pro Val Ser Gly Leu Val Ala Ala Asp 165 170 175 Tyr Phe Ala Pro Gly Tyr Phe Val Trp Ala Val Leu Ile Ala Asn Leu 180 185 190 Ala Arg Val Gly Tyr Glu Glu Lys Asn Met Tyr Met Ala Ala Tyr Asp 195 200 205 Trp Arg Leu Ser Phe Gln Asn Thr Glu Val Arg Asp Gln Thr Leu Ser 210 215 220 Arg Ile Lys Ser Asn Ile Glu Leu Met Val Ala Thr Asn Gly Gly Lys 225 230 235 240 Lys Ala Val Ile Ile Pro His Ser Met Gly Val Ile Tyr Phe Leu His 245 250 255 Phe Met Lys Trp Val Glu Ala Pro Ala Pro Met Gly Gly Gly Gly Gly 260 265 270 Pro Asp Trp Cys Ala Lys His Ile Lys Ala Val Met Asn Ile Gly Gly 275 280 285 Pro Phe Leu Gly Val Pro Lys Ala Val Ala Gly Leu Phe Ser Ala Glu 290 295 300 Ala Lys Asp Ile Ala Ser Val Arg Ala Leu Ala Pro Gly Met Leu Asp 305 310 315 320 Ser Asp Leu Phe Gln Ile Gln Thr Leu Gln His Ile Met Arg Met Ser 325 330 335 Arg Thr Trp Asp Ser Thr Met Ser Met Ile Pro Lys Gly Gly Asp Thr 340 345 350 Ile Trp Gly Gly Leu Asp Trp Ser Pro Glu Asp Gly Tyr Ser Pro Ser 355 360 365 Lys Arg Lys His Gly Lys Asn Asp Thr Glu Ser Ser Thr Gln Asn Glu 370 375 380 Ser Ala Ser Glu Glu Cys Glu Val Thr His Ala Asn Tyr Gly Arg Ile 385 390 395 400 Val Ser Phe Gly Arg Asp Val Ala Glu Ala Pro Ser Ser Glu Ile Glu 405 410 415 Arg Ile Glu Phe Arg Gly Ala Val Lys Gly Asn Asn Val Ala Asn Asn 420 425 430 Thr Cys Arg Ala Val Trp Thr Glu Tyr His Asp Met Gly Phe Gly Gly 435 440 445 Ile Lys Ala Val Ala Glu Tyr Lys Val Tyr Thr Ala Gly Glu Ile Val 450 455 460 Asp Met Leu Glu Phe Val Ala Pro Lys Met Met Glu Arg Gly Ser Ala 465 470 475 480 His Phe Ser Tyr Gly Ile Ala Asp Asn Leu Asp Asp Pro Lys Tyr Ser 485 490 495 His Tyr Lys Tyr Trp Ser Asn Pro Leu Glu Thr Lys Leu Pro Asn Ala 500 505 510 Pro Asp Met Glu Ile Tyr Ser Met Tyr Gly Val Gly Ile Pro Thr Glu 515 520 525 Arg Ala Tyr Val Tyr Lys Leu Thr Pro Ala Ala Glu Cys Tyr Ile Pro 530 535 540 Phe Gln Ile Asp Thr Ser Ala Lys Asp Lys Asn Glu Asp Gly Cys Leu 545 550 555 560 Lys Asp Gly Val Tyr Thr Val Asp Gly Asp Glu Thr Val Pro Ala Leu 565 570 575 Ser Ala Gly Tyr Met Cys Ala Lys Gly Trp Arg Gly Lys Thr Arg Phe 580 585 590 Asn Pro Ser Gly Ile Lys Thr Tyr Val Arg Glu Tyr Asp His Asn Pro 595 600 605 Pro Ser Asn Phe Leu Glu Gly Arg Gly Thr Gln Ser Gly Ala His Val 610 615 620 Asp Ile Met Gly Asn Phe Gln Leu Ile Glu Asp Val Ile Lys Val Ala 625 630 635 640 Ala Gly Ala Thr Gly Glu Glu Leu Gly Gly Asp Gln Val Tyr Thr Gly 645 650 655 Ile Phe Glu Trp Ser Glu Lys Ile Asn Leu Glu Leu 660 665 19 2565 DNA Zea mays 19 cgcgacctca caagcgcgaa ccccacgaag ccggagccaa gccacgacgg gtcgaccggt 60 cgacggcccc tcgacctgcc cgcctcgctt cctccgacgc ctagggtttt ctaccggacg 120 ccgccgccgc cgcagcagcg gcccgggatg caggtgtgcc cgcgcagtta gccgccgtcg 180 gacccaccgc cgccgcgcgc catgtcattc ttgcggcggc gaaagccgct gccgccctct 240 gacggtgacg agtccgacca cgacgacaac gacaagggga agaagccgtc ctcatcctcc 300 gggtcgccgt ccaaggagcc cacgaagcgg accaaggcca agtggtcgtg cgtggacagc 360 tgctgctggc tggtcgggtg cgtgtgctcc gcctggtggt tgctgctctt tctctacaac 420 gcgatgccag cttcgttccc gcagtatgta acggaggcca tcacgggtcc gctcccggac 480 ccgcccgggg tcaagctgca gaaggagggg ctgcgagcta agcaccccgt cgtctttgtc 540 cccggcatcg tcaccggggg cctcgagcta tgggagggac accaatgcgc cgagggtctc 600 ttccgcaagc ggctatgggg cggcacattt ggtgacgtat acaagagacc tctatgctgg 660 gttgaacata tgtcgttgga caatgaaact ggattagaca aacctggaat aagggtcagg 720 tcagtcacag gccttgttgc agcagactat ttcgtccccg gatattttgt ttgggctgtc 780 ttaattgcca atttagctcg tattggatat gaagaaaaga ccatgtacat ggctgcatat 840 gattggaggt tatctttcca gaacactgag gttcgtgatc aaactttgag cagaataaag 900 agcaatattg aactcatggt agcaacaaat ggtggaaata gggtggtggt gatcccacac 960 tccatggggg tcctctattt tctgcatttt atgaaatggg tcgaagcacc tcctcccatg 1020 gggggcggtg gtggtccgaa ctggtgtgag aagcatatta aagctgtaat gaatattgga 1080 ggacctttct taggagttcc caaggctgtt gctgggcttt tctcatctga agccaaagat 1140 gttgccgttg ctagagctat cgctcctgat gtcctggact ctgattttct tggacttcaa 1200 actttgcgcc atttgatgcg tatgacccga acatgggatt caacaatgtc aatgcttcct 1260 aaaggtggtg atacaatttg gggaaatctg gattggtctc cagaagatgg ccttgaatgt 1320 aaagctaaga agcataaaac caatgatacc gaggtttcta aggatagcaa tggggaaaat 1380 atcgaagttc aacctgaacc tataaactac ggaaggctgg tatccttcgg taaagatgta 1440 gcagaggcac cttcttcaga gattgaacag atagaatttc gtgatgctgt taaaggtaac 1500 gatatcgtcc attcaaatgc atcatgccgg gagatctgga cagagtacca tgaattagga 1560 tggggtggaa taaaggcagt cgcagactac aaagtttaca ctgccagttc tgttatagac 1620 cttcttcact ttgttgctcc aaggatgatg cagcgtggaa atgtccactt ttcatatgga 1680 attgctgata acttggatga tccgaaatat caacattaca aatattggtc aaaccccttg 1740 gaaacaaagc taccgaatgc tcctgacatg gaaataattt ccatgtacgg agtaggcatt 1800 cctactgaaa gggcatatgt ctacaagttg gctccacagg cagagtgcta tataccattc 1860 cggattgacg cctcggctga tggcggggag gaaaacaaat gcttgaaagg gggtgtttac 1920 ttagctgacg gcgacgaaac tgttccagtt cttagcgcgg gctacatgtg tgcaaaaggg 1980 tggcgtggca aaactcgttt caaccctgcc ggcagcaaga cttacgtgag agagtacagc 2040 cattcaccac cctcaactct cctggaaggc aggggcactc agagcggtgc acatgttgat 2100 ataatgggga acttcgcttt gatcgaggac atcatcagga tagctgccgg ggcaaccggt 2160 gaggaaattg gtggcgacca ggtttattca gatatattca aatggtcaga gaaaatcaaa 2220 ttgaaattgt aacccatggg aagttaaaag aagtgcccca acccgttcat tgcgttccta 2280 aatgcttgcc tgagcgcaac tctggatttt gcttaaatat cgtatttttt tcacgcctca 2340 ttcgtccctc tagtaaattt acattgacag gaccccggtg cgacgcggat gttgtaccgt 2400 atttttggca ttgtatatta aaatgtacag gcgtaagtta catttgctag ctgaaattat 2460 tgcagtagct tgccttttct tttgagcacg gaaaaaaaaa aaaaaaaaaa aaaaaaaaaa 2520 aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaa 2565 20 676 PRT Zea mays 20 Met Ser Phe Leu Arg Arg Arg Lys Pro Leu Pro Pro Ser Asp Gly Asp 1 5 10 15 Glu Ser Asp His Asp Asp Asn Asp Lys Gly Lys Lys Pro Ser Ser Ser 20 25 30 Ser Gly Ser Pro Ser Lys Glu Pro Thr Lys Arg Thr Lys Ala Lys Trp 35 40 45 Ser Cys Val Asp Ser Cys Cys Trp Leu Val Gly Cys Val Cys Ser Ala 50 55 60 Trp Trp Leu Leu Leu Phe Leu Tyr Asn Ala Met Pro Ala Ser Phe Pro 65 70 75 80 Gln Tyr Val Thr Glu Ala Ile Thr Gly Pro Leu Pro Asp Pro Pro Gly 85 90 95 Val Lys Leu Gln Lys Glu Gly Leu Arg Ala Lys His Pro Val Val Phe 100 105 110 Val Pro Gly Ile Val Thr Gly Gly Leu Glu Leu Trp Glu Gly His Gln 115 120 125 Cys Ala Glu Gly Leu Phe Arg Lys Arg Leu Trp Gly Gly Thr Phe Gly 130 135 140 Asp Val Tyr Lys Arg Pro Leu Cys Trp Val Glu His Met Ser Leu Asp 145 150 155 160 Asn Glu Thr Gly Leu Asp Lys Pro Gly Ile Arg Val Arg Ser Val Thr 165 170 175 Gly Leu Val Ala Ala Asp Tyr Phe Val Pro Gly Tyr Phe Val Trp Ala 180 185 190 Val Leu Ile Ala Asn Leu Ala Arg Ile Gly Tyr Glu Glu Lys Thr Met 195 200 205 Tyr Met Ala Ala Tyr Asp Trp Arg Leu Ser Phe Gln Asn Thr Glu Val 210 215 220 Arg Asp Gln Thr Leu Ser Arg Ile Lys Ser Asn Ile Glu Leu Met Val 225 230 235 240 Ala Thr Asn Gly Gly Asn Arg Val Val Val Ile Pro His Ser Met Gly 245 250 255 Val Leu Tyr Phe Leu His Phe Met Lys Trp Val Glu Ala Pro Pro Pro 260 265 270 Met Gly Gly Gly Gly Gly Pro Asn Trp Cys Glu Lys His Ile Lys Ala 275 280 285 Val Met Asn Ile Gly Gly Pro Phe Leu Gly Val Pro Lys Ala Val Ala 290 295 300 Gly Leu Phe Ser Ser Glu Ala Lys Asp Val Ala Val Ala Arg Ala Ile 305 310 315 320 Ala Pro Asp Val Leu Asp Ser Asp Phe Leu Gly Leu Gln Thr Leu Arg 325 330 335 His Leu Met Arg Met Thr Arg Thr Trp Asp Ser Thr Met Ser Met Leu 340 345 350 Pro Lys Gly Gly Asp Thr Ile Trp Gly Asn Leu Asp Trp Ser Pro Glu 355 360 365 Asp Gly Leu Glu Cys Lys Ala Lys Lys His Lys Thr Asn Asp Thr Glu 370 375 380 Val Ser Lys Asp Ser Asn Gly Glu Asn Ile Glu Val Gln Pro Glu Pro 385 390 395 400 Ile Asn Tyr Gly Arg Leu Val Ser Phe Gly Lys Asp Val Ala Glu Ala 405 410 415 Pro Ser Ser Glu Ile Glu Gln Ile Glu Phe Arg Asp Ala Val Lys Gly 420 425 430 Asn Asp Ile Val His Ser Asn Ala Ser Cys Arg Glu Ile Trp Thr Glu 435 440 445 Tyr His Glu Leu Gly Trp Gly Gly Ile Lys Ala Val Ala Asp Tyr Lys 450 455 460 Val Tyr Thr Ala Ser Ser Val Ile Asp Leu Leu His Phe Val Ala Pro 465 470 475 480 Arg Met Met Gln Arg Gly Asn Val His Phe Ser Tyr Gly Ile Ala Asp 485 490 495 Asn Leu Asp Asp Pro Lys Tyr Gln His Tyr Lys Tyr Trp Ser Asn Pro 500 505 510 Leu Glu Thr Lys Leu Pro Asn Ala Pro Asp Met Glu Ile Ile Ser Met 515 520 525 Tyr Gly Val Gly Ile Pro Thr Glu Arg Ala Tyr Val Tyr Lys Leu Ala 530 535 540 Pro Gln Ala Glu Cys Tyr Ile Pro Phe Arg Ile Asp Ala Ser Ala Asp 545 550 555 560 Gly Gly Glu Glu Asn Lys Cys Leu Lys Gly Gly Val Tyr Leu Ala Asp 565 570 575 Gly Asp Glu Thr Val Pro Val Leu Ser Ala Gly Tyr Met Cys Ala Lys 580 585 590 Gly Trp Arg Gly Lys Thr Arg Phe Asn Pro Ala Gly Ser Lys Thr Tyr 595 600 605 Val Arg Glu Tyr Ser His Ser Pro Pro Ser Thr Leu Leu Glu Gly Arg 610 615 620 Gly Thr Gln Ser Gly Ala His Val Asp Ile Met Gly Asn Phe Ala Leu 625 630 635 640 Ile Glu Asp Ile Ile Arg Ile Ala Ala Gly Ala Thr Gly Glu Glu Ile 645 650 655 Gly Gly Asp Gln Val Tyr Ser Asp Ile Phe Lys Trp Ser Glu Lys Ile 660 665 670 Lys Leu Lys Leu 675 21 2433 DNA Oryza sativa 21 ttcggcacga ggtttaaacc aagcgcgaac cccgcggagc cgccacctct ctcgcctccc 60 cgcctccgcc gcgccgccta gggtttccac cgcccccggg atgcgcgcgc cccctcgccg 120 gtagcctccc ccccggttcc cgccgcctcc gccgccgcca tgtcgctgct gcggcgccgg 180 aagcagccgc agccgccgcc ggagcagccg aacgaggaca gcagcaacgg ctccgacctc 240 gacgagaagg ggaagaagaa gccgggatcg tcgtcctcct cggcggcgcc tcctccggag 300 gcggcggcgg cggcggcgaa ggaggcgacg aagcggacga gggccaggtg gtcgtgcgtg 360 gacagctgct gctggctggt ggggtgcgtg tgctcggcgt ggtggctgct gctcttcctg 420 tacaacgcga tgccggcgtc gttcccgcag tacgtcacgg aggcgatcac ggggccgctc 480 ccggaccctc ccggggtcaa gctgcagaag gaggggctgc gggcgaagca ccccgtcgtg 540 ttcgtcccgg gcatcgtcac cggcggcctc gagctctggg aggggcacca gtgcgccgag 600 gggctcttcc gcaagcgcct ctggggcggc acgttcggcg acgtgtacaa gaggccttta 660 tgctgggttg aacatatgtc actggacaat gaaactggat tagataaacc aggaataaga 720 gttcggccag tcacaggcct agtggcagca gactattttg ttcctgggta ttttgtttgg 780 gctgttttga ttgcaaattt agctcgtatt ggatatgaag aaaagaccat gtacatggct 840 gcatatgatt ggaggttatc tttccagaac actgaggttc gtgatcaaac tttgagcagg 900 ataaaaagta acattgaact cctggtagca actaatggtg gaaatagggt ggtggtgatc 960 ccacattcta tgggggttct ctattttctg cattttatga agtgggttga ggctcctcct 1020 cccatgggtg gtggtggtgg tccaaattgg tgtgcaaagc acatcaaatc tgtaatgaat 1080 attggcggac ctttcttagg agttcctaag gctgttgcag gacttttctc atctgaagcc 1140 aaagatgttg ctgttgctag agccattgca ccagaagtcc tagactctga cttccttgga 1200 cttcagacct tacgccattt gatgcgtatg acccgcacat gggattcaac aatgtcaatg 1260 attcctaagg gcggtgacac catttgggga gatttggatt ggtctccaga agatggtttt 1320 gagtgtaaag ctaagaatca gaaaatcaat gattctgagg tttctaagga tgctaacggg 1380 aagaatgagg ttcatccaga acctgttaag tatggaagaa ttgtctcttt cggtaaagat 1440 gtagcagagg ctccatcttc agaaattgag cagatagaat ttcgtgatgc tgtcaaaggc 1500 aataatattg cccactcaaa tacatcatgc cgggatatat ggacagagta tcacgaatta 1560 ggatggggcg gaataaaggc agttgcagac tacaaggttt acactgctgg ctccattata 1620 gatcttcttc gttttgttgc tccaaggatg atgcagcgtg gaagtgttca cttttcgtat 1680 gggattgctg acaacttgga tgatccaaag tacggccact acaaatactg gtcaaatccc 1740 ttggaaacaa aattaccaaa tgcacctgaa atggaaatat tttcaatgta tggagttggc 1800 attccgacgg agagagcata tgtctataaa ttagccccac aagcagagtg ctatatacct 1860 tttcagatag acgcttcagc tgagggtggg gatgagaata gctgtctgaa aggcggcgtt 1920 tacctgtcta atggtgatga gaccgtacca gttcttagtg caggatatat gtgcgcaaaa 1980 ggctggcgag gaaaaacacg cttcaaccct tctggcagca agacctacgt cagagaatac 2040 agccattctc caccctcaaa tctcctcgaa ggcaggggca cccagagtgg tgcgcacgtt 2100 gatatcatgg ggaattttgc tttaatcgag gatattatca ggattgctgc tggggcaact 2160 ggtgaagagc ttggcggtga ccaggtttat tccgatatat tcaaatggtc tgataagatt 2220 aaattgaaac tataaaactt taaaaaagca tggtagtttt gtaggagaat tatttgtttc 2280 ctggccaaaa ttttatgagt tttgattcga tattgtaata tgattttttt tacctttccc 2340 ttaagctctt aattcagtag aggctgactt gatttgtatt attttgtgat ttgagcggca 2400 ttgtatatta aaaaaaaaaa aaaaaaaaaa aaa 2433 22 691 PRT Oryza sativa 22 Met Ser Leu Leu Arg Arg Arg Lys Gln Pro Gln Pro Pro Pro Glu Gln 1 5 10 15 Pro Asn Glu Asp Ser Ser Asn Gly Ser Asp Leu Asp Glu Lys Gly Lys 20 25 30 Lys Lys Pro Gly Ser Ser Ser Ser Ser Ala Ala Pro Pro Pro Glu Ala 35 40 45 Ala Ala Ala Ala Ala Lys Glu Ala Thr Lys Arg Thr Arg Ala Arg Trp 50 55 60 Ser Cys Val Asp Ser Cys Cys Trp Leu Val Gly Cys Val Cys Ser Ala 65 70 75 80 Trp Trp Leu Leu Leu Phe Leu Tyr Asn Ala Met Pro Ala Ser Phe Pro 85 90 95 Gln Tyr Val Thr Glu Ala Ile Thr Gly Pro Leu Pro Asp Pro Pro Gly 100 105 110 Val Lys Leu Gln Lys Glu Gly Leu Arg Ala Lys His Pro Val Val Phe 115 120 125 Val Pro Gly Ile Val Thr Gly Gly Leu Glu Leu Trp Glu Gly His Gln 130 135 140 Cys Ala Glu Gly Leu Phe Arg Lys Arg Leu Trp Gly Gly Thr Phe Gly 145 150 155 160 Asp Val Tyr Lys Arg Pro Leu Cys Trp Val Glu His Met Ser Leu Asp 165 170 175 Asn Glu Thr Gly Leu Asp Lys Pro Gly Ile Arg Val Arg Pro Val Thr 180 185 190 Gly Leu Val Ala Ala Asp Tyr Phe Val Pro Gly Tyr Phe Val Trp Ala 195 200 205 Val Leu Ile Ala Asn Leu Ala Arg Ile Gly Tyr Glu Glu Lys Thr Met 210 215 220 Tyr Met Ala Ala Tyr Asp Trp Arg Leu Ser Phe Gln Asn Thr Glu Val 225 230 235 240 Arg Asp Gln Thr Leu Ser Arg Ile Lys Ser Asn Ile Glu Leu Leu Val 245 250 255 Ala Thr Asn Gly Gly Asn Arg Val Val Val Ile Pro His Ser Met Gly 260 265 270 Val Leu Tyr Phe Leu His Phe Met Lys Trp Val Glu Ala Pro Pro Pro 275 280 285 Met Gly Gly Gly Gly Gly Pro Asn Trp Cys Ala Lys His Ile Lys Ser 290 295 300 Val Met Asn Ile Gly Gly Pro Phe Leu Gly Val Pro Lys Ala Val Ala 305 310 315 320 Gly Leu Phe Ser Ser Glu Ala Lys Asp Val Ala Val Ala Arg Ala Ile 325 330 335 Ala Pro Glu Val Leu Asp Ser Asp Phe Leu Gly Leu Gln Thr Leu Arg 340 345 350 His Leu Met Arg Met Thr Arg Thr Trp Asp Ser Thr Met Ser Met Ile 355 360 365 Pro Lys Gly Gly Asp Thr Ile Trp Gly Asp Leu Asp Trp Ser Pro Glu 370 375 380 Asp Gly Phe Glu Cys Lys Ala Lys Asn Gln Lys Ile Asn Asp Ser Glu 385 390 395 400 Val Ser Lys Asp Ala Asn Gly Lys Asn Glu Val His Pro Glu Pro Val 405 410 415 Lys Tyr Gly Arg Ile Val Ser Phe Gly Lys Asp Val Ala Glu Ala Pro 420 425 430 Ser Ser Glu Ile Glu Gln Ile Glu Phe Arg Asp Ala Val Lys Gly Asn 435 440 445 Asn Ile Ala His Ser Asn Thr Ser Cys Arg Asp Ile Trp Thr Glu Tyr 450 455 460 His Glu Leu Gly Trp Gly Gly Ile Lys Ala Val Ala Asp Tyr Lys Val 465 470 475 480 Tyr Thr Ala Gly Ser Ile Ile Asp Leu Leu Arg Phe Val Ala Pro Arg 485 490 495 Met Met Gln Arg Gly Ser Val His Phe Ser Tyr Gly Ile Ala Asp Asn 500 505 510 Leu Asp Asp Pro Lys Tyr Gly His Tyr Lys Tyr Trp Ser Asn Pro Leu 515 520 525 Glu Thr Lys Leu Pro Asn Ala Pro Glu Met Glu Ile Phe Ser Met Tyr 530 535 540 Gly Val Gly Ile Pro Thr Glu Arg Ala Tyr Val Tyr Lys Leu Ala Pro 545 550 555 560 Gln Ala Glu Cys Tyr Ile Pro Phe Gln Ile Asp Ala Ser Ala Glu Gly 565 570 575 Gly Asp Glu Asn Ser Cys Leu Lys Gly Gly Val Tyr Leu Ser Asn Gly 580 585 590 Asp Glu Thr Val Pro Val Leu Ser Ala Gly Tyr Met Cys Ala Lys Gly 595 600 605 Trp Arg Gly Lys Thr Arg Phe Asn Pro Ser Gly Ser Lys Thr Tyr Val 610 615 620 Arg Glu Tyr Ser His Ser Pro Pro Ser Asn Leu Leu Glu Gly Arg Gly 625 630 635 640 Thr Gln Ser Gly Ala His Val Asp Ile Met Gly Asn Phe Ala Leu Ile 645 650 655 Glu Asp Ile Ile Arg Ile Ala Ala Gly Ala Thr Gly Glu Glu Leu Gly 660 665 670 Gly Asp Gln Val Tyr Ser Asp Ile Phe Lys Trp Ser Asp Lys Ile Lys 675 680 685 Leu Lys Leu 690 23 2700 DNA Glycine max 23 gccgcacctt ccaaaattgt tgataagttt ctccttgttt ctcgaaaaaa tcagaggaaa 60 gagattccgg atcagtttcc gttcagtggt tcacagatgc tataaccaat agtcatcatc 120 ttcagaaaaa aaccaccttt tttttgccat tctgagctca ccgagctacc caatgcgatt 180 ttgattcgcg ggcttttcat ttctgtataa atctgcaatc tttgaggaaa ataacgtaac 240 cccatctgtt tataatcata tggggcacaa gtgaacggaa actctcgagg aaattgaggt 300 ttgaagcttg taacgcatcc tagaatatta tgtctttgct tcgacggaga aaagggtcgg 360 aaccggaaaa gggtccgagc ccgagttcgg agccaaaggt tttaagcgaa gacgagacag 420 aagatgataa gaataataag aagaataaga agaagagaga tgaggtgggg gagaagaaga 480 agaacaaatg gtcatgcttc gatagctgtt gttggtgggt ggggtgcatt tgcacattgt 540 ggtggtttct tctgtttctg tatcagatga tgccttcttc gattcctcag tatgtgaccg 600 aggccttcac tgggcccatg ccggacccac cgggcctcaa actcaaaaag gaaggactca 660 aggtgaagca ccctgtggtt tttgtgcccg ggattgtcac tggggggctt gaactgtggg 720 agggtcacct gtgtgctgag gggttgttca ggaaacgctt gtggggtggt acttttggag 780 aagtctataa aagaccttca tgctgggtgg atcacatgtc actggacaat gaaacaggat 840 tggatccacc aggcataaga gttaggcctg tctctggact tgtagctgct gattactttg 900 ctgcaggata cttcgtttgg gcagtcctaa ttgctaactt ggcacgcatt ggttatgaag 960 aaaaaactat gtacatggct gcatatgatt ggagaatagc atttcagaac actgaggtga 1020 gggatcaaac actaagtcgg ataaaaagca acatagaact tatggttgct actaatggtg 1080 gaaataaggc agttattatt ccacattcaa tgggggtctt gtacttccta cattttatga 1140 aatgggttga agcaccagct ccaatgggtg gtgggggagg accagattgg tgctccaaat 1200 atataaaggc agttgtaaac attggtggac catttttagg tgttcccaag gctatagcag 1260 ggctattctc agctgaggcc agggatattg ctgttgccag gacgatagct ccaggatttt 1320 tagataacga tctgtttcgc attcaaacct tgcaacatgt aatgaagatg acccgtactt 1380 gggactcaac aatgtcaatg ataccaagag gaggagatac tatatggggt ggtcttgatt 1440 ggtcaccaga agaaggctat caccctagcc agaggaagca tagcagtgac tatactcagt 1500 taacagacca agagacaaat caaacaaatg ttgtcaacta tggaagaatg atatcatttg 1560 gcagagatgt ggccgaggca cactcctcta agattgagat ggctgacttt cggggtgcca 1620 tcaagggtcg cagtgttgca aataccacct gtcgtgatgt gtggactgaa taccatgaaa 1680 tgggatttga gggagtgaga gcagttgctg aacataaagt ttacacagct ggctctatcg 1740 tagaactcct tcaatttgtt gctccaaaga tgatggctcg tggtagtgct catttctctt 1800 atgaaattgc tgacaatttg gatgacccta aatataatca ctacaagtat tggtcaaacc 1860 ctttggaaac aaaactacca aatgctcctg atatggaaat cttctctatg tatggagttg 1920 gcttaccaac tgaaagatct tatatttaca agttaactcc ctttgccgag tgttacattc 1980 cttttgaaat tgacaccacg caagatggtg gaagtgatga agatagttgt ctgcaaggtg 2040 gagtctacac tgttgatggg gatgagactg tgccagttct aagttcaggc tacatgtgtg 2100 ctaaaggctg gcgcggaaaa acaagattca acccgtctgg tatgcgcacc tacgttagag 2160 aatatgatca ttctcctcca gccaaccttc tagagggaag gggcacacaa agtggtgctc 2220 atgttgacat catgggaaac tttgcattga ttgaggatgt tataagagtg gctgctggag 2280 ccaaaggaga agatctagga ggtgataaag tgtattctga tatcttcaag tggtctgaga 2340 aaatcaagtt acccctatga atgaagcaca atgtaattcc gcagttccac tcagacacac 2400 ttctcttgaa cccctttaag gatcagatca gactatatat aattttttgc agtatatttt 2460 cactgccacc agagttctat gagttgctgg ttctgctgat caaagtccag ttccatggag 2520 gggtgaacta cgcgaattgg ttatattgga agagcttgca ttgaacattt ttgttattaa 2580 agtaaggatt ttatttgtca tctctaagaa acctgaccgg gggcattatt cttaataagt 2640 tcagctgatt agttatgata aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa 2700 24 676 PRT Glycine max 24 Met Ser Leu Leu Arg Arg Arg Lys Gly Ser Glu Pro Glu Lys Gly Pro 1 5 10 15 Ser Pro Ser Ser Glu Pro Lys Val Leu Ser Glu Asp Glu Thr Glu Asp 20 25 30 Asp Lys Asn Asn Lys Lys Asn Lys Lys Lys Arg Asp Glu Val Gly Glu 35 40 45 Lys Lys Lys Asn Lys Trp Ser Cys Phe Asp Ser Cys Cys Trp Trp Val 50 55 60 Gly Cys Ile Cys Thr Leu Trp Trp Phe Leu Leu Phe Leu Tyr Gln Met 65 70 75 80 Met Pro Ser Ser Ile Pro Gln Tyr Val Thr Glu Ala Phe Thr Gly Pro 85 90 95 Met Pro Asp Pro Pro Gly Leu Lys Leu Lys Lys Glu Gly Leu Lys Val 100 105 110 Lys His Pro Val Val Phe Val Pro Gly Ile Val Thr Gly Gly Leu Glu 115 120 125 Leu Trp Glu Gly His Leu Cys Ala Glu Gly Leu Phe Arg Lys Arg Leu 130 135 140 Trp Gly Gly Thr Phe Gly Glu Val Tyr Lys Arg Pro Ser Cys Trp Val 145 150 155 160 Asp His Met Ser Leu Asp Asn Glu Thr Gly Leu Asp Pro Pro Gly Ile 165 170 175 Arg Val Arg Pro Val Ser Gly Leu Val Ala Ala Asp Tyr Phe Ala Ala 180 185 190 Gly Tyr Phe Val Trp Ala Val Leu Ile Ala Asn Leu Ala Arg Ile Gly 195 200 205 Tyr Glu Glu Lys Thr Met Tyr Met Ala Ala Tyr Asp Trp Arg Ile Ala 210 215 220 Phe Gln Asn Thr Glu Val Arg Asp Gln Thr Leu Ser Arg Ile Lys Ser 225 230 235 240 Asn Ile Glu Leu Met Val Ala Thr Asn Gly Gly Asn Lys Ala Val Ile 245 250 255 Ile Pro His Ser Met Gly Val Leu Tyr Phe Leu His Phe Met Lys Trp 260 265 270 Val Glu Ala Pro Ala Pro Met Gly Gly Gly Gly Gly Pro Asp Trp Cys 275 280 285 Ser Lys Tyr Ile Lys Ala Val Val Asn Ile Gly Gly Pro Phe Leu Gly 290 295 300 Val Pro Lys Ala Ile Ala Gly Leu Phe Ser Ala Glu Ala Arg Asp Ile 305 310 315 320 Ala Val Ala Arg Thr Ile Ala Pro Gly Phe Leu Asp Asn Asp Leu Phe 325 330 335 Arg Ile Gln Thr Leu Gln His Val Met Lys Met Thr Arg Thr Trp Asp 340 345 350 Ser Thr Met Ser Met Ile Pro Arg Gly Gly Asp Thr Ile Trp Gly Gly 355 360 365 Leu Asp Trp Ser Pro Glu Glu Gly Tyr His Pro Ser Gln Arg Lys His 370 375 380 Ser Ser Asp Tyr Thr Gln Leu Thr Asp Gln Glu Thr Asn Gln Thr Asn 385 390 395 400 Val Val Asn Tyr Gly Arg Met Ile Ser Phe Gly Arg Asp Val Ala Glu 405 410 415 Ala His Ser Ser Lys Ile Glu Met Ala Asp Phe Arg Gly Ala Ile Lys 420 425 430 Gly Arg Ser Val Ala Asn Thr Thr Cys Arg Asp Val Trp Thr Glu Tyr 435 440 445 His Glu Met Gly Phe Glu Gly Val Arg Ala Val Ala Glu His Lys Val 450 455 460 Tyr Thr Ala Gly Ser Ile Val Glu Leu Leu Gln Phe Val Ala Pro Lys 465 470 475 480 Met Met Ala Arg Gly Ser Ala His Phe Ser Tyr Glu Ile Ala Asp Asn 485 490 495 Leu Asp Asp Pro Lys Tyr Asn His Tyr Lys Tyr Trp Ser Asn Pro Leu 500 505 510 Glu Thr Lys Leu Pro Asn Ala Pro Asp Met Glu Ile Phe Ser Met Tyr 515 520 525 Gly Val Gly Leu Pro Thr Glu Arg Ser Tyr Ile Tyr Lys Leu Thr Pro 530 535 540 Phe Ala Glu Cys Tyr Ile Pro Phe Glu Ile Asp Thr Thr Gln Asp Gly 545 550 555 560 Gly Ser Asp Glu Asp Ser Cys Leu Gln Gly Gly Val Tyr Thr Val Asp 565 570 575 Gly Asp Glu Thr Val Pro Val Leu Ser Ser Gly Tyr Met Cys Ala Lys 580 585 590 Gly Trp Arg Gly Lys Thr Arg Phe Asn Pro Ser Gly Met Arg Thr Tyr 595 600 605 Val Arg Glu Tyr Asp His Ser Pro Pro Ala Asn Leu Leu Glu Gly Arg 610 615 620 Gly Thr Gln Ser Gly Ala His Val Asp Ile Met Gly Asn Phe Ala Leu 625 630 635 640 Ile Glu Asp Val Ile Arg Val Ala Ala Gly Ala Lys Gly Glu Asp Leu 645 650 655 Gly Gly Asp Lys Val Tyr Ser Asp Ile Phe Lys Trp Ser Glu Lys Ile 660 665 670 Lys Leu Pro Leu 675 25 2398 DNA Helianthus sp. 25 ccacgcgtcc gcaccactct ccgccgcttg cacacgtcac cacctcaact ccacacgtca 60 cgcttcttca tccatcctct aaccgcttca atccgactta ctaatggcgt tactccgaag 120 aagaaaacaa ccagattccg atccacatcc ggatccgggt caggatccga aaccagatga 180 agaagacgat aaggaacaaa aagcgtcaaa aaaatcaaac aaaaacggta aaataaagaa 240 ctattcgtgc ctcgataact gctgttggtt cgtcggttgc gtgtgctcgg tgtggtggtt 300 gttgttgttt ttgtataatg ctatgccggc gtcgttcccg cagtttgtga cggaagcgat 360 atccggaccg tttccggatc ctcccggagt taagtgtttg aaagaaggtt tgaaggcgaa 420 gcatccggtg gtgtttgtgc cggggattgt gaccggtgga cttgagctgt gggaagggca 480 ccagtgtatg gatggattgt tccggaaaag gctttggggc ggtacgtttg gtgaggttta 540 taagaggcct tcgtgttggg tacaacatat gtcgctagac aacaaaaccg ggatggatcc 600 accgggtata cgggtcaggc ctgtcagtgg acttgtagct gctgactact tcgctccagg 660 gtattttgtt tgggctgttt tgattgctaa cttggcacgt gttggctatg aagagaaaaa 720 tatgtatatg gctgcatatg actggagact ctcgtttcaa aacacagagg taagagacca 780 aacactgagc cggataaaga gcaatataga actgatggtt gctactaatg gcgggaaaaa 840 ggcggttatc atcccgcatt caatgggtgt tatctacttc ctgcatttca tgaaatgggt 900 cgaggcacca gcaccaatgg gtggcggagg tggaccagat tggtgtgcta aacacataaa 960 agcggtgatg aatatcggtg gaccattttt aggtgtccca aaagctgtag ccgggctttt 1020 ctctgcggaa gctaaagata ttgcatcagt cagggccctt gcaccaggtg tgttagactc 1080 ggatttattt cagattcaaa cgttacaaca tgtaatgaga atgagccgca catgggattc 1140 aaccatgtct atgataccga aaggcgggga caccatttgg ggcggcctca attggtcacc 1200 cgaagaaggg tatagtccaa ggaggagtaa acatggaaaa aacgacactg aatctcccac 1260 cgtaagtgat tctgcaagtg aagtaacaca tgcaaattat ggaaggatag tatcgttcgg 1320 gagagatgta gcagaggcac catcttcaga gatcgagagg atagaattta gaggtgctgt 1380 gaagggtatc aatgttgcaa acaatacatg tcgggccgtg tggaccgaat accatgacat 1440 gggatttggt ggaatcaagg ctgttgcgga gtacaaggta tatacagctg gcgaaatcgt 1500 ggaactgctg gagtttgttg ctccaaaaat gatggaacgc ggtagtgctc atttttcgta 1560 tggtattgct gacaatttgg atgatccaaa atatacacat tacaagtatt ggtctaaccc 1620 attggagaca aagttaccaa acgctccaga catggagatc tattcaatgt atggagttgg 1680 catcccaacc gaaagagcat atgtctacaa actcacacct gcggcagagt gctacatacc 1740 attccaaatt gacacgtcag caaaggataa aggcgaggac gggtgtttaa aagacggggt 1800 ttatacggtt gacggggatg aaacagtacc agcactaagc gcgggttaca tgtgcgcaaa 1860 gggttggcgt gggaaaacgc gattcaatcc ttcgggaatt aaaacttatg tcagggaata 1920 cgatcacaac cctccatcca actttctcga gggccggggc actcaaagcg gggcccatgt 1980 ggatattatg ggtaattttc agttgattga agatgttata agagttgcag ccggagccac 2040 gggtgaagaa cttggaggtg atcaggtgta cactggtata ttcgagtggt ccgagaagat 2100 caatctaaag ttgtgaaata tgtgacttag attttataca aacagtatat cagggtgcgt 2160 ttgttacata gttttgatta gagatctgcg atacatggaa gattattgtg tcatatttaa 2220 accaataagg gttagtgcgc ttcttgcagt tctctacttg aatttgtcta tgtattaagc 2280 gtgaactcta tgtgcattat tgatccacaa atctgtattg tgggtggatt attttgtaat 2340 atgtagcatg ttgcttcctt gaacagccaa aaaaaaaaaa aaaaaaaaaa aaaaaaaa 2398 26 670 PRT Helianthus sp. 26 Met Ala Leu Leu Arg Arg Arg Lys Gln Pro Asp Ser Asp Pro His Pro 1 5 10 15 Asp Pro Gly Gln Asp Pro Lys Pro Asp Glu Glu Asp Asp Lys Glu Gln 20 25 30 Lys Ala Ser Lys Lys Ser Asn Lys Asn Gly Lys Ile Lys Asn Tyr Ser 35 40 45 Cys Leu Asp Asn Cys Cys Trp Phe Val Gly Cys Val Cys Ser Val Trp 50 55 60 Trp Leu Leu Leu Phe Leu Tyr Asn Ala Met Pro Ala Ser Phe Pro Gln 65 70 75 80 Phe Val Thr Glu Ala Ile Ser Gly Pro Phe Pro Asp Pro Pro Gly Val 85 90 95 Lys Cys Leu Lys Glu Gly Leu Lys Ala Lys His Pro Val Val Phe Val 100 105 110 Pro Gly Ile Val Thr Gly Gly Leu Glu Leu Trp Glu Gly His Gln Cys 115 120 125 Met Asp Gly Leu Phe Arg Lys Arg Leu Trp Gly Gly Thr Phe Gly Glu 130 135 140 Val Tyr Lys Arg Pro Ser Cys Trp Val Gln His Met Ser Leu Asp Asn 145 150 155 160 Lys Thr Gly Met Asp Pro Pro Gly Ile Arg Val Arg Pro Val Ser Gly 165 170 175 Leu Val Ala Ala Asp Tyr Phe Ala Pro Gly Tyr Phe Val Trp Ala Val 180 185 190 Leu Ile Ala Asn Leu Ala Arg Val Gly Tyr Glu Glu Lys Asn Met Tyr 195 200 205 Met Ala Ala Tyr Asp Trp Arg Leu Ser Phe Gln Asn Thr Glu Val Arg 210 215 220 Asp Gln Thr Leu Ser Arg Ile Lys Ser Asn Ile Glu Leu Met Val Ala 225 230 235 240 Thr Asn Gly Gly Lys Lys Ala Val Ile Ile Pro His Ser Met Gly Val 245 250 255 Ile Tyr Phe Leu His Phe Met Lys Trp Val Glu Ala Pro Ala Pro Met 260 265 270 Gly Gly Gly Gly Gly Pro Asp Trp Cys Ala Lys His Ile Lys Ala Val 275 280 285 Met Asn Ile Gly Gly Pro Phe Leu Gly Val Pro Lys Ala Val Ala Gly 290 295 300 Leu Phe Ser Ala Glu Ala Lys Asp Ile Ala Ser Val Arg Ala Leu Ala 305 310 315 320 Pro Gly Val Leu Asp Ser Asp Leu Phe Gln Ile Gln Thr Leu Gln His 325 330 335 Val Met Arg Met Ser Arg Thr Trp Asp Ser Thr Met Ser Met Ile Pro 340 345 350 Lys Gly Gly Asp Thr Ile Trp Gly Gly Leu Asn Trp Ser Pro Glu Glu 355 360 365 Gly Tyr Ser Pro Arg Arg Ser Lys His Gly Lys Asn Asp Thr Glu Ser 370 375 380 Pro Thr Val Ser Asp Ser Ala Ser Glu Val Thr His Ala Asn Tyr Gly 385 390 395 400 Arg Ile Val Ser Phe Gly Arg Asp Val Ala Glu Ala Pro Ser Ser Glu 405 410 415 Ile Glu Arg Ile Glu Phe Arg Gly Ala Val Lys Gly Ile Asn Val Ala 420 425 430 Asn Asn Thr Cys Arg Ala Val Trp Thr Glu Tyr His Asp Met Gly Phe 435 440 445 Gly Gly Ile Lys Ala Val Ala Glu Tyr Lys Val Tyr Thr Ala Gly Glu 450 455 460 Ile Val Glu Leu Leu Glu Phe Val Ala Pro Lys Met Met Glu Arg Gly 465 470 475 480 Ser Ala His Phe Ser Tyr Gly Ile Ala Asp Asn Leu Asp Asp Pro Lys 485 490 495 Tyr Thr His Tyr Lys Tyr Trp Ser Asn Pro Leu Glu Thr Lys Leu Pro 500 505 510 Asn Ala Pro Asp Met Glu Ile Tyr Ser Met Tyr Gly Val Gly Ile Pro 515 520 525 Thr Glu Arg Ala Tyr Val Tyr Lys Leu Thr Pro Ala Ala Glu Cys Tyr 530 535 540 Ile Pro Phe Gln Ile Asp Thr Ser Ala Lys Asp Lys Gly Glu Asp Gly 545 550 555 560 Cys Leu Lys Asp Gly Val Tyr Thr Val Asp Gly Asp Glu Thr Val Pro 565 570 575 Ala Leu Ser Ala Gly Tyr Met Cys Ala Lys Gly Trp Arg Gly Lys Thr 580 585 590 Arg Phe Asn Pro Ser Gly Ile Lys Thr Tyr Val Arg Glu Tyr Asp His 595 600 605 Asn Pro Pro Ser Asn Phe Leu Glu Gly Arg Gly Thr Gln Ser Gly Ala 610 615 620 His Val Asp Ile Met Gly Asn Phe Gln Leu Ile Glu Asp Val Ile Arg 625 630 635 640 Val Ala Ala Gly Ala Thr Gly Glu Glu Leu Gly Gly Asp Gln Val Tyr 645 650 655 Thr Gly Ile Phe Glu Trp Ser Glu Lys Ile Asn Leu Lys Leu 660 665 670 27 2030 DNA Triticum aestivum 27 ctcgtgccga attcggcacg agcggaggcc atcacgggcc cgctcccgga cccgcccggg 60 gtcaagctgc agaaggaggg gctgcacgcc aagcaccccg tcatcttcgt gccggggatc 120 gtcaccggag ggctcgagct ctgggagggc caccactgcg ccgaggggct cttccggaag 180 cgcctctggg gcggcacatt cggcgacgtg tacaagaggc ctttatgctg gattgaacat 240 atgtcattgg acaacgaaac tggattagat aaaccaggaa taagagttag gccagtcaca 300 ggccttgtcg cagctgacta ttttgtccct ggctattttg tttgggcagt cctgattgcc 360 aatttagctc ggattggata tgaagaaaag aacatgtaca tggctgctta tgattggagg 420 ttatcattcc agaacactga gacccgtgat caaacattga gcagaataaa gagtaacatt 480 gagctcttgg tagcgactaa tggtggaaat agggcggtgg tgatcccaca ttccatggga 540 gttctctatt ttcttcattt tatgaagtgg gtagaagcac cttctcccat gggtggtggt 600 ggtggtcctg attggtgtgc aaagcacatc aaagctgtag caaacattgg tgggcctttc 660 ttaggagttc caaaggctgt tgctgggctt ttctcatctg aagccaaaga tgttgctgtt 720 gctagagcta ttgcaccaga aatgctggac tcagattttc ttggacttca gaccttgcgc 780 cacttgatgc gaatgacccg tacatgggat tcaacaatgt caatgctccc taaaggtggt 840 gagactattt ggggaggttt ggattggtct ccagaagatg gttttgagtg taaatccaag 900 aagcggaaga ccaatgattc agaggtttct aaggatgttc atggggaacc tgtcgaagtt 960 aatccagagc ctgtgaactt tggaagaatg gtatcttttg gaaaagatgt agcggaagct 1020 ccggcttcaa atattgagca gatagaattc cgtgatgctg tcaaaggtaa taatcttgcc 1080 cattcgaata catcatgccg ggatgtctgg acagagtatc aggaattagg gtggggtgga 1140 ataaaggcag tttcagacta caaagctttc accgcaggct ctatcataga tctttttaac 1200 tttgttgctc caaggatgat gcagcgtggt agtgttcatt tttcatatgg aattgctgat 1260 aacttggatg atccaaaata tggccactac aagtattggt caaacccctt ggagacaaaa 1320 ctaccagatg cgcctgaaat ggaaatattt tcgatgtatg gagtaggcat tcctaccgaa 1380 agagcatatg tctataaatt atccccacag gcagagtgct atataccctt tcagatagat 1440 gcctcagctg agggtgggga tgagaatagc tgcttgaaag gtggtgttta catgtcgaat 1500 ggtgacgaga ctgttccagt tcttagttca gggtatatgt gtgccaaagc atggcgtgga 1560 aaaactcgct tcaacccttc tggcagcaag acttacgtga gagagtatag tcattctcca 1620 ccctcgaatc tcctcgaagg caggggcaca cagagtggtg cccacgttga tattatgggg 1680 aactttgctt taatggagga tattatcagg attgctgctg gggcaaccgg tgaggaaatt 1740 ggtggtgatc aggtgtattc tgatatattc aaatggtccg agaagataaa gctgaaattg 1800 tagttagtag gaaatcatgt gatttgtggt gacgaagcag attttactct ggtcgaatcc 1860 tattaatttt gatttgataa tgtaatggtt tttgctctga cactggcgtt attgtgaaac 1920 cgcggtgtat attaaaatgt atagatggaa gctgtgatac ttctgttaaa aaaaaaaaaa 1980 aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa 2030 28 600 PRT Triticum aestivum 28 Leu Val Pro Asn Ser Ala Arg Ala Glu Ala Ile Thr Gly Pro Leu Pro 1 5 10 15 Asp Pro Pro Gly Val Lys Leu Gln Lys Glu Gly Leu His Ala Lys His 20 25 30 Pro Val Ile Phe Val Pro Gly Ile Val Thr Gly Gly Leu Glu Leu Trp 35 40 45 Glu Gly His His Cys Ala Glu Gly Leu Phe Arg Lys Arg Leu Trp Gly 50 55 60 Gly Thr Phe Gly Asp Val Tyr Lys Arg Pro Leu Cys Trp Ile Glu His 65 70 75 80 Met Ser Leu Asp Asn Glu Thr Gly Leu Asp Lys Pro Gly Ile Arg Val 85 90 95 Arg Pro Val Thr Gly Leu Val Ala Ala Asp Tyr Phe Val Pro Gly Tyr 100 105 110 Phe Val Trp Ala Val Leu Ile Ala Asn Leu Ala Arg Ile Gly Tyr Glu 115 120 125 Glu Lys Asn Met Tyr Met Ala Ala Tyr Asp Trp Arg Leu Ser Phe Gln 130 135 140 Asn Thr Glu Thr Arg Asp Gln Thr Leu Ser Arg Ile Lys Ser Asn Ile 145 150 155 160 Glu Leu Leu Val Ala Thr Asn Gly Gly Asn Arg Ala Val Val Ile Pro 165 170 175 His Ser Met Gly Val Leu Tyr Phe Leu His Phe Met Lys Trp Val Glu 180 185 190 Ala Pro Ser Pro Met Gly Gly Gly Gly Gly Pro Asp Trp Cys Ala Lys 195 200 205 His Ile Lys Ala Val Ala Asn Ile Gly Gly Pro Phe Leu Gly Val Pro 210 215 220 Lys Ala Val Ala Gly Leu Phe Ser Ser Glu Ala Lys Asp Val Ala Val 225 230 235 240 Ala Arg Ala Ile Ala Pro Glu Met Leu Asp Ser Asp Phe Leu Gly Leu 245 250 255 Gln Thr Leu Arg His Leu Met Arg Met Thr Arg Thr Trp Asp Ser Thr 260 265 270 Met Ser Met Leu Pro Lys Gly Gly Glu Thr Ile Trp Gly Gly Leu Asp 275 280 285 Trp Ser Pro Glu Asp Gly Phe Glu Cys Lys Ser Lys Lys Arg Lys Thr 290 295 300 Asn Asp Ser Glu Val Ser Lys Asp Val His Gly Glu Pro Val Glu Val 305 310 315 320 Asn Pro Glu Pro Val Asn Phe Gly Arg Met Val Ser Phe Gly Lys Asp 325 330 335 Val Ala Glu Ala Pro Ala Ser Asn Ile Glu Gln Ile Glu Phe Arg Asp 340 345 350 Ala Val Lys Gly Asn Asn Leu Ala His Ser Asn Thr Ser Cys Arg Asp 355 360 365 Val Trp Thr Glu Tyr Gln Glu Leu Gly Trp Gly Gly Ile Lys Ala Val 370 375 380 Ser Asp Tyr Lys Ala Phe Thr Ala Gly Ser Ile Ile Asp Leu Phe Asn 385 390 395 400 Phe Val Ala Pro Arg Met Met Gln Arg Gly Ser Val His Phe Ser Tyr 405 410 415 Gly Ile Ala Asp Asn Leu Asp Asp Pro Lys Tyr Gly His Tyr Lys Tyr 420 425 430 Trp Ser Asn Pro Leu Glu Thr Lys Leu Pro Asp Ala Pro Glu Met Glu 435 440 445 Ile Phe Ser Met Tyr Gly Val Gly Ile Pro Thr Glu Arg Ala Tyr Val 450 455 460 Tyr Lys Leu Ser Pro Gln Ala Glu Cys Tyr Ile Pro Phe Gln Ile Asp 465 470 475 480 Ala Ser Ala Glu Gly Gly Asp Glu Asn Ser Cys Leu Lys Gly Gly Val 485 490 495 Tyr Met Ser Asn Gly Asp Glu Thr Val Pro Val Leu Ser Ser Gly Tyr 500 505 510 Met Cys Ala Lys Ala Trp Arg Gly Lys Thr Arg Phe Asn Pro Ser Gly 515 520 525 Ser Lys Thr Tyr Val Arg Glu Tyr Ser His Ser Pro Pro Ser Asn Leu 530 535 540 Leu Glu Gly Arg Gly Thr Gln Ser Gly Ala His Val Asp Ile Met Gly 545 550 555 560 Asn Phe Ala Leu Met Glu Asp Ile Ile Arg Ile Ala Ala Gly Ala Thr 565 570 575 Gly Glu Glu Ile Gly Gly Asp Gln Val Tyr Ser Asp Ile Phe Lys Trp 580 585 590 Ser Glu Lys Ile Lys Leu Lys Leu 595 600 29 493 PRT Arabidopsis thaliana 29 Met Ser Leu Leu Leu Glu Glu Ile Ile Arg Ser Val Glu Ala Leu Leu 1 5 10 15 Lys Leu Arg Asn Arg Asn Gln Glu Pro Tyr Val Asp Pro Asn Leu Asn 20 25 30 Pro Val Leu Leu Val Pro Gly Ile Ala Gly Ser Ile Leu Asn Ala Val 35 40 45 Asp His Glu Asn Gly Asn Glu Glu Arg Val Trp Val Arg Ile Phe Gly 50 55 60 Ala Asp His Glu Phe Arg Thr Lys Met Trp Ser Arg Phe Asp Pro Ser 65 70 75 80 Thr Gly Lys Thr Ile Ser Leu Asp Pro Lys Thr Ser Ile Val Val Pro 85 90 95 Gln Asp Arg Ala Gly Leu His Ala Ile Asp Val Leu Asp Pro Asp Met 100 105 110 Ile Val Gly Arg Glu Ser Val Tyr Tyr Phe His Glu Met Ile Val Glu 115 120 125 Met Ile Gly Trp Gly Phe Glu Glu Gly Lys Thr Leu Phe Gly Phe Gly 130 135 140 Tyr Asp Phe Arg Gln Ser Asn Arg Leu Gln Glu Thr Leu Asp Gln Phe 145 150 155 160 Ala Lys Lys Leu Glu Thr Val Tyr Lys Ala Ser Gly Glu Lys Lys Ile 165 170 175 Asn Val Ile Ser His Ser Met Gly Gly Leu Leu Val Lys Cys Phe Met 180 185 190 Gly Leu His Ser Asp Val Cys Lys Ser Leu Phe Leu Tyr Ser Tyr Ser 195 200 205 Arg Ser Met Tyr Arg Ile Gly Leu Leu Leu Leu Leu His Phe Glu Val 210 215 220 Ser Ser Leu Thr Cys Gly Thr Ser Asp Ser Thr Gly Asp Asn Tyr His 225 230 235 240 Thr Asp Trp Phe Arg Ile Ile Asp Ser Gly Ala Pro Gly Tyr Ile Thr 245 250 255 Ser Thr Leu Leu Asn Gly Met Ser Phe Val Asn Gly Trp Glu Gln Asn 260 265 270 Phe Phe Val Ser Lys Trp Ser Met His Gln Leu Ser Cys Gly Glu Arg 275 280 285 Lys Arg Ala Met Met Glu Leu Glu Pro Leu Met Leu Phe Leu Ser Leu 290 295 300 Thr Val Ala Trp Arg Ala Leu Lys Phe Leu Arg Asn Leu Phe Arg Ile 305 310 315 320 Ile His Tyr Gly Asn Glu Lys Met Pro Val Lys Asp Leu Thr Asn Leu 325 330 335 Arg Tyr Phe Gln Pro Thr Tyr Ile Cys Val Asp Gly Asp Gly Thr Val 340 345 350 Pro Met Glu Ser Ala Met Ala Asp Gly Leu Glu Ala Val Ala Arg Val 355 360 365 Gly Val Pro Gly Glu His Arg Gly Ile Leu Asn Asp His Arg Val Phe 370 375 380 Arg Met Leu Lys Lys Trp Leu Asn Val Gly Glu Pro Asp Pro Phe Tyr 385 390 395 400 Asn Pro Val Asn Asp Tyr Val Ile Leu Pro Thr Thr Tyr Glu Phe Glu 405 410 415 Lys Phe His Glu Asn Gly Leu Glu Val Ala Ser Val Lys Glu Ser Trp 420 425 430 Asp Ile Ile Ser Asp Asp Asn Asn Ile Gly Thr Thr Gly Ser Thr Val 435 440 445 Asn Ser Ile Ser Val Ser Gln Pro Gly Asp Asp Gln Asn Pro Gln Ala 450 455 460 Glu Ala Arg Ala Thr Leu Thr Val Gln Pro Gln Ser Asp Gly Arg Gln 465 470 475 480 His Val Glu Leu Asn Ala Val Ser Val Ser Val Asp Ala 485 490 30 671 PRT Arabidopsis thaliana 30 Met Pro Leu Ile His Arg Lys Lys Pro Thr Glu Lys Pro Ser Thr Pro 1 5 10 15 Pro Ser Glu Glu Val Val His Asp Glu Asp Ser Gln Lys Lys Pro His 20 25 30 Glu Ser Ser Lys Ser His His Lys Lys Ser Asn Gly Gly Gly Lys Trp 35 40 45 Ser Cys Ile Asp Ser Cys Cys Trp Phe Ile Gly Cys Val Cys Val Thr 50 55 60 Trp Trp Phe Leu Leu Phe Leu Tyr Asn Ala Met Pro Ala Ser Phe Pro 65 70 75 80 Gln Tyr Val Thr Glu Arg Ile Thr Gly Pro Leu Pro Asp Pro Pro Gly 85 90 95 Val Lys Leu Lys Lys Glu Gly Leu Lys Ala Lys His Pro Val Val Phe 100 105 110 Ile Pro Gly Ile Val Thr Gly Gly Leu Glu Leu Trp Glu Gly Lys Gln 115 120 125 Cys Ala Asp Gly Leu Phe Arg Lys Arg Leu Trp Gly Gly Thr Phe Gly 130 135 140 Glu Val Tyr Lys Arg Pro Leu Cys Trp Val Glu His Met Ser Leu Asp 145 150 155 160 Asn Glu Thr Gly Leu Asp Pro Ala Gly Ile Arg Val Arg Ala Val Ser 165 170 175 Gly Leu Val Ala Ala Asp Tyr Phe Ala Pro Gly Tyr Phe Val Trp Ala 180 185 190 Val Leu Ile Ala Asn Leu Ala His Ile Gly Tyr Glu Glu Lys Asn Met 195 200 205 Tyr Met Ala Ala Tyr Asp Trp Arg Leu Ser Phe Gln Asn Thr Glu Val 210 215 220 Arg Asp Gln Thr Leu Ser Arg Met Lys Ser Asn Ile Glu Leu Met Val 225 230 235 240 Ser Thr Asn Gly Gly Lys Lys Ala Val Ile Val Pro His Ser Met Gly 245 250 255 Val Leu Tyr Phe Leu His Phe Met Lys Trp Val Glu Ala Pro Ala Pro 260 265 270 Leu Gly Gly Gly Gly Gly Pro Asp Trp Cys Ala Lys Tyr Ile Lys Ala 275 280 285 Val Met Asn Ile Gly Gly Pro Phe Leu Gly Val Pro Lys Ala Val Ala 290 295 300 Gly Leu Phe Ser Ala Glu Ala Lys Asp Val Ala Val Ala Arg Ala Ile 305 310 315 320 Ala Pro Gly Phe Leu Asp Thr Asp Ile Phe Arg Leu Gln Thr Leu Gln 325 330 335 His Val Met Arg Met Thr Arg Thr Trp Asp Ser Thr Met Ser Met Leu 340 345 350 Pro Lys Gly Gly Asp Thr Ile Trp Gly Gly Leu Asp Trp Ser Pro Glu 355 360 365 Lys Gly His Thr Cys Cys Gly Lys Lys Gln Lys Asn Asn Glu Thr Cys 370 375 380 Gly Glu Ala Gly Glu Asn Gly Val Ser Lys Lys Ser Pro Val Asn Tyr 385 390 395 400 Gly Arg Met Ile Ser Phe Gly Lys Glu Val Ala Glu Ala Ala Pro Ser 405 410 415 Glu Ile Asn Asn Ile Asp Phe Arg Gly Ala Val Lys Gly Gln Ser Ile 420 425 430 Pro Asn His Thr Cys Arg Asp Val Trp Thr Glu Tyr His Asp Met Gly 435 440 445 Ile Ala Gly Ile Lys Ala Ile Ala Glu Tyr Lys Val Tyr Thr Ala Gly 450 455 460 Glu Ala Ile Asp Leu Leu His Tyr Val Ala Pro Lys Met Met Ala Arg 465 470 475 480 Gly Ala Ala His Phe Ser Tyr Gly Ile Ala Asp Asp Leu Asp Asp Thr 485 490 495 Lys Tyr Gln Asp Pro Lys Tyr Trp Ser Asn Pro Leu Glu Thr Lys Leu 500 505 510 Pro Asn Ala Pro Glu Met Glu Ile Tyr Ser Leu Tyr Gly Val Gly Ile 515 520 525 Pro Thr Glu Arg Ala Tyr Val Tyr Lys Leu Asn Gln Ser Pro Asp Ser 530 535 540 Cys Ile Pro Phe Gln Ile Phe Thr Ser Ala His Glu Glu Asp Glu Asp 545 550 555 560 Ser Cys Leu Lys Ala Gly Val Tyr Asn Val Asp Gly Asp Glu Thr Val 565 570 575 Pro Val Leu Ser Ala Gly Tyr Met Cys Ala Lys Ala Trp Arg Gly Lys 580 585 590 Thr Arg Phe Asn Pro Ser Gly Ile Lys Thr Tyr Ile Arg Glu Tyr Asn 595 600 605 His Ser Pro Pro Ala Asn Leu Leu Glu Gly Arg Gly Thr Gln Ser Gly 610 615 620 Ala His Val Asp Ile Met Gly Asn Phe Ala Leu Ile Glu Asp Ile Met 625 630 635 640 Arg Val Ala Ala Gly Gly Asn Gly Ser Asp Ile Gly His Asp Gln Val 645 650 655 His Ser Gly Ile Phe Glu Trp Ser Glu Arg Ile Asp Leu Lys Leu 660 665 670 31 1957 DNA C. tetragonoloba 31 gcacgagggt taacagcacc ttcacctaat agaaacccta tttcccaatt cgatttccgg 60 tgaattatcc attctggaaa ctcccgatca atcaattggt tgttgttagg gtttccattt 120 gcagatggcg atcttgttgg acgagatcct acaatccttg gagttatggc tgaagctgat 180 caagaagccc cagccagagc cctacatcaa ccctaatcta gaccctgttt tattggtgcc 240 tggaatcggt ggctccatgt tgcatgctgt aagcgattcc aacggcaaca gagaacgggt 300 ttgggttcgc ttcctcggcg cggattacat gttgaggacc aagctttggt cacgttacga 360 tccttctacc ggaaaatcca tatccttgga tacaaataca acaattttga ttcctgaaga 420 taggcatgga ctttatgcaa ttgatgtttt ggaccccgac ttggtaattg gaagcgagtc 480 tgtttattat ttccatgaca tgatcgtgga aatgcgcaaa tgggggtatc aagagggaaa 540 gacacttttt ggctttggat atgattttcg acaaagcaac aggttgcagg aaacaataga 600 tcggttggct gcaaaattag aatcaattta tgatgctgct ggagggaaaa agataaacat 660 cataagtcat tctatgggcg gtcttttggt gaaatgtttc atgtgcctgc aaagtgatat 720 ttttgagaaa tgtgttaaga attgggttgc aattgctgca ccattccagg gtgcacctgg 780 atgtatcaat tctaccttgt taaatggaat gtcatttgta gatggatggg agcaaaaggt 840 ttacatttcc aaatggagca tgcaccagtt gctgattgaa tgtccatcaa tttacgaact 900 tatgggttgt cctaattttc attggcaaca tattcctctt ctggaattgt ggcgtgagag 960 acatgattct gatgggaaat ctggtattat tctggaatca tatccaccgt gtgatagcgt 1020 tgaggttttg aagcaagctc ttgtaaataa cacagttaat tataatggtg aggatttacc 1080 ccttcccttc aacacagaga tcttgaaatg ggccaaaaaa acttgggaga tcctgtcttc 1140 tgccaaactt cctccaaatg ttaaatttta caatatttat gggactaatc tcgagacggc 1200 tcatagcatt tgctatggaa gtgcagacaa gcctgtctca gatctgcagc agctacgtta 1260 ttaccagccc aaatacgtat gtgttgatgg cgacggaaca gttccggtag aatcagctaa 1320 ggctgacggg ctcaatgcgg aggcgagggt tggagtccca ggcgaacatc gaggtatcct 1380 tcgtgaccct catgtattca ggattctcaa gcactggcta aaggctggag atcctgatcc 1440 cttttacaac cctctcaatg attatgtgat tctacctact gcttttgaaa tggagagtca 1500 taaagagaaa ggtttagaag tagcatccct taaagaggag tgggaaatta tttccaaaga 1560 ccaagatgaa caacaaagca atattgctga agaaatgtct ctgagtacca tatcagtttc 1620 gcatgaagga gccaatcaat cttgttccga ggctcatgct actgtcgtcg ttcgcccagg 1680 cgatgagggt aaacaacaca ttcaactgaa tgtcgttgct gtttcagtcg atgcctcatg 1740 aatccatgtg ttgaagaaga atgagtgaag gtggagggaa atacttgcta catagttgat 1800 tgtgggtgat ttctcttgta tataaggata ttcgattgat gctgctgctg ccatattctt 1860 ccttgtatga tatacgatat accaatatgt atcattggaa aaaaataatt aaaagaaaag 1920 aaaaatacca tcttctatga caaaaaaaaa aaaaaaa 1957 32 538 PRT C. tetragonoloba 32 Met Ala Ile Leu Leu Asp Glu Ile Leu Gln Ser Leu Glu Leu Trp Leu 1 5 10 15 Lys Leu Ile Lys Lys Pro Gln Pro Glu Pro Tyr Ile Asn Pro Asn Leu 20 25 30 Asp Pro Val Leu Leu Val Pro Gly Ile Gly Gly Ser Met Leu His Ala 35 40 45 Val Ser Asp Ser Asn Gly Asn Arg Glu Arg Val Trp Val Arg Phe Leu 50 55 60 Gly Ala Asp Tyr Met Leu Arg Thr Lys Leu Trp Ser Arg Tyr Asp Pro 65 70 75 80 Ser Thr Gly Lys Ser Ile Ser Leu Asp Thr Asn Thr Thr Ile Leu Ile 85 90 95 Pro Glu Asp Arg His Gly Leu Tyr Ala Ile Asp Val Leu Asp Pro Asp 100 105 110 Leu Val Ile Gly Ser Glu Ser Val Tyr Tyr Phe His Asp Met Ile Val 115 120 125 Glu Met Arg Lys Trp Gly Tyr Gln Glu Gly Lys Thr Leu Phe Gly Phe 130 135 140 Gly Tyr Asp Phe Arg Gln Ser Asn Arg Leu Gln Glu Thr Ile Asp Arg 145 150 155 160 Leu Ala Ala Lys Leu Glu Ser Ile Tyr Asp Ala Ala Gly Gly Lys Lys 165 170 175 Ile Asn Ile Ile Ser His Ser Met Gly Gly Leu Leu Val Lys Cys Phe 180 185 190 Met Cys Leu Gln Ser Asp Ile Phe Glu Lys Cys Val Lys Asn Trp Val 195 200 205 Ala Ile Ala Ala Pro Phe Gln Gly Ala Pro Gly Cys Ile Asn Ser Thr 210 215 220 Leu Leu Asn Gly Met Ser Phe Val Asp Gly Trp Glu Gln Lys Val Tyr 225 230 235 240 Ile Ser Lys Trp Ser Met His Gln Leu Leu Ile Glu Cys Pro Ser Ile 245 250 255 Tyr Glu Leu Met Gly Cys Pro Asn Phe His Trp Gln His Ile Pro Leu 260 265 270 Leu Glu Leu Trp Arg Glu Arg His Asp Ser Asp Gly Lys Ser Gly Ile 275 280 285 Ile Leu Glu Ser Tyr Pro Pro Cys Asp Ser Val Glu Val Leu Lys Gln 290 295 300 Ala Leu Val Asn Asn Thr Val Asn Tyr Asn Gly Glu Asp Leu Pro Leu 305 310 315 320 Pro Phe Asn Thr Glu Ile Leu Lys Trp Ala Lys Lys Thr Trp Glu Ile 325 330 335 Leu Ser Ser Ala Lys Leu Pro Pro Asn Val Lys Phe Tyr Asn Ile Tyr 340 345 350 Gly Thr Asn Leu Glu Thr Ala His Ser Ile Cys Tyr Gly Ser Ala Asp 355 360 365 Lys Pro Val Ser Asp Leu Gln Gln Leu Arg Tyr Tyr Gln Pro Lys Tyr 370 375 380 Val Cys Val Asp Gly Asp Gly Thr Val Pro Val Glu Ser Ala Lys Ala 385 390 395 400 Asp Gly Leu Asn Ala Glu Ala Arg Val Gly Val Pro Gly Glu His Arg 405 410 415 Gly Ile Leu Arg Asp Pro His Val Phe Arg Ile Leu Lys His Trp Leu 420 425 430 Lys Ala Gly Asp Pro Asp Pro Phe Tyr Asn Pro Leu Asn Asp Tyr Val 435 440 445 Ile Leu Pro Thr Ala Phe Glu Met Glu Ser His Lys Glu Lys Gly Leu 450 455 460 Glu Val Ala Ser Leu Lys Glu Glu Trp Glu Ile Ile Ser Lys Asp Gln 465 470 475 480 Asp Glu Gln Gln Ser Asn Ile Ala Glu Glu Met Ser Leu Ser Thr Ile 485 490 495 Ser Val Ser His Glu Gly Ala Asn Gln Ser Cys Ser Glu Ala His Ala 500 505 510 Thr Val Val Val Arg Pro Gly Asp Glu Gly Lys Gln His Ile Gln Leu 515 520 525 Asn Val Val Ala Val Ser Val Asp Ala Ser 530 535 33 2077 DNA Triticum aestivum 33 cgcctccgga atccccaccc ccgtccaaat ccgggcaaac catatacccc agctacccgc 60 cgcggagcag attccccgcc atccgccgac gccacgccac gccacccccg tgccgctccg 120 attcgagctt gccggagctc ggtttggccg gaagcctcgc cctctcatgc tgatctcgcg 180 gccgggggct tgagagtgct tatttagggc ggggatttgg gcggcgggga agcaaggatg 240 tcggtgctgg aggatttgat ccgggcgatc gagctgtggc tgcggatcgc caaggagcag 300 gtgccgctgg tcgaccccag cctcgacccg gtgctgctcg tgcccggcat cggcggctcc 360 atcctcgagg ccgtggacga ggccgggaac aaggagcggg tctgggtgcg catcctcgcc 420 gccgaccacg agtgccgcga gaagctctgg gcgcagttcg atgcctccac tggcaaaact 480 atttctgtgg atgagaaaat acgcatcact gtcccggagg ataggtatgg attgtacgcc 540 atcgacacat tggacccaga cctgattatt ggtgatgaca gtgtttacta ctatcatgac 600 atgatagtgc aaatgattaa atggggatat caagaaggca aaactctgtt cggatttggt 660 tatgatttcc gccaaagtaa caggctttcg gaaacacttg acaaattttc taacaagcta 720 gagtcagtat acacagcttc aggagggaaa aagatcaatc taataacaca ttcaatgggg 780 ggattgcttg ttaaatgctt catgtctctt catggtgatg tctttgaaaa atatgtgaag 840 agttgggttg caattgctgc accatttcaa ggtgcgcctg ggtacataaa tagtggtctg 900 ctgaatggaa tgtcttttgt ggaaggatgg caatcaaaat tcttcatttc caaatggact 960 atgcagcaat tgttgattga atgtccatca atatacgagt tgttggctag ctcaacctac 1020 cactgggaag atacaccatt gctacagatc tggaaagaga gcttagatga caatggcaag 1080 aaaagtgcca tactggagtc ctatgaacca gatgaagcaa taaagatgat tcagaaagct 1140 ctttccaagc atgagattat ctctgatgga aatcacattc ctctgcccct taatgaggat 1200 atattaatat gggcaaagga aactcaagat atcttatccc aggcaaagct tccaaaatca 1260 gtgaagttct acaatattta cgggattgat tatgacactg ctcatactgt ttgctacggg 1320 agcaaacggc accctatttc aaatcttagt cacctcttat atactcaggg taaatacatc 1380 tgtgttgatg gtgatggatc cgttcccgca gaatcagcaa aggcggacgg ccttgatgca 1440 gtggcgagaa ttggggttgc tgctgaccac cgaggaatcg tctgcgacca ccgcgtgttt 1500 cgcatagtcc agcattggct gcacgcgggt gaacctgacc cgttttacga cccgctcaac 1560 gactatgtcg tcatcccaac catcttcgag gtcgagaagc accacgagaa acgcggggac 1620 gtcacgtcgg tcagggagga ctgggagatc atctcccaca ccgatggcga cgaggccaaa 1680 aggctggctg agctccctgc tatggttggc gcgatgtctg cgtcttgcga gggtaaggat 1740 ggccttatgg acgaggcgca ggccaccgtg gtggtccacc cggagagcgg agggcggcag 1800 catgtggaag tcagggctgt cggagtcagc cacggtggct agctatgggc ctactcgccg 1860 tataacttta gctagggcga ttgcacatac tgtaaaccgt tgatgcacat aagatgtggc 1920 caagtaggga atatgtctct gtaaatacgg tatactgctg cttgtaaata tctgaacttg 1980 gaagcacaag gtgcactggc tatgagcacc aaggaggaag gaaataatca gaatggatta 2040 ccagcttgtc accttgtaaa aaaaaaaaaa aaaaaaa 2077 34 534 PRT Triticum aestivum 34 Met Ser Val Leu Glu Asp Leu Ile Arg Ala Ile Glu Leu Trp Leu Arg 1 5 10 15 Ile Ala Lys Glu Gln Val Pro Leu Val Asp Pro Ser Leu Asp Pro Val 20 25 30 Leu Leu Val Pro Gly Ile Gly Gly Ser Ile Leu Glu Ala Val Asp Glu 35 40 45 Ala Gly Asn Lys Glu Arg Val Trp Val Arg Ile Leu Ala Ala Asp His 50 55 60 Glu Cys Arg Glu Lys Leu Trp Ala Gln Phe Asp Ala Ser Thr Gly Lys 65 70 75 80 Thr Ile Ser Val Asp Glu Lys Ile Arg Ile Thr Val Pro Glu Asp Arg 85 90 95 Tyr Gly Leu Tyr Ala Ile Asp Thr Leu Asp Pro Asp Leu Ile Ile Gly 100 105 110 Asp Asp Ser Val Tyr Tyr Tyr His Asp Met Ile Val Gln Met Ile Lys 115 120 125 Trp Gly Tyr Gln Glu Gly Lys Thr Leu Phe Gly Phe Gly Tyr Asp Phe 130 135 140 Arg Gln Ser Asn Arg Leu Ser Glu Thr Leu Asp Lys Phe Ser Asn Lys 145 150 155 160 Leu Glu Ser Val Tyr Thr Ala Ser Gly Gly Lys Lys Ile Asn Leu Ile 165 170 175 Thr His Ser Met Gly Gly Leu Leu Val Lys Cys Phe Met Ser Leu His 180 185 190 Gly Asp Val Phe Glu Lys Tyr Val Lys Ser Trp Val Ala Ile Ala Ala 195 200 205 Pro Phe Gln Gly Ala Pro Gly Tyr Ile Asn Ser Gly Leu Leu Asn Gly 210 215 220 Met Ser Phe Val Glu Gly Trp Gln Ser Lys Phe Phe Ile Ser Lys Trp 225 230 235 240 Thr Met Gln Gln Leu Leu Ile Glu Cys Pro Ser Ile Tyr Glu Leu Leu 245 250 255 Ala Ser Ser Thr Tyr His Trp Glu Asp Thr Pro Leu Leu Gln Ile Trp 260 265 270 Lys Glu Ser Leu Asp Asp Asn Gly Lys Lys Ser Ala Ile Leu Glu Ser 275 280 285 Tyr Glu Pro Asp Glu Ala Ile Lys Met Ile Gln Lys Ala Leu Ser Lys 290 295 300 His Glu Ile Ile Ser Asp Gly Asn His Ile Pro Leu Pro Leu Asn Glu 305 310 315 320 Asp Ile Leu Ile Trp Ala Lys Glu Thr Gln Asp Ile Leu Ser Gln Ala 325 330 335 Lys Leu Pro Lys Ser Val Lys Phe Tyr Asn Ile Tyr Gly Ile Asp Tyr 340 345 350 Asp Thr Ala His Thr Val Cys Tyr Gly Ser Lys Arg His Pro Ile Ser 355 360 365 Asn Leu Ser His Leu Leu Tyr Thr Gln Gly Lys Tyr Ile Cys Val Asp 370 375 380 Gly Asp Gly Ser Val Pro Ala Glu Ser Ala Lys Ala Asp Gly Leu Asp 385 390 395 400 Ala Val Ala Arg Ile Gly Val Ala Ala Asp His Arg Gly Ile Val Cys 405 410 415 Asp His Arg Val Phe Arg Ile Val Gln His Trp Leu His Ala Gly Glu 420 425 430 Pro Asp Pro Phe Tyr Asp Pro Leu Asn Asp Tyr Val Val Ile Pro Thr 435 440 445 Ile Phe Glu Val Glu Lys His His Glu Lys Arg Gly Asp Val Thr Ser 450 455 460 Val Arg Glu Asp Trp Glu Ile Ile Ser His Thr Asp Gly Asp Glu Ala 465 470 475 480 Lys Arg Leu Ala Glu Leu Pro Ala Met Val Gly Ala Met Ser Ala Ser 485 490 495 Cys Glu Gly Lys Asp Gly Leu Met Asp Glu Ala Gln Ala Thr Val Val 500 505 510 Val His Pro Glu Ser Gly Gly Arg Gln His Val Glu Val Arg Ala Val 515 520 525 Gly Val Ser His Gly Gly 530 35 4093 DNA Glycine max 35 gattccggat cagtttccgt tcagtggttc acagatgcta taaccaatag tcatcatctt 60 cagaaaaaaa ccaccttttt ttgccattct gagctcaccg agctacccaa tgcgattttg 120 attcgcgggc ttttcatttc tgtataaatc tgcaatcttt gaggaaaata acgtaacccc 180 atctgtttat aatcatatgg ggcacaagtg aacggaaact ctcgaggaaa ttgaggtttg 240 aagcttgtaa cgcatcctag aatattatgt ctttgcttcg acggagaaaa gggtcggaac 300 cggaaaaggg tccgagcccg agttcggagc caaaggtttt aagcgaagac gagacagaag 360 atgataagaa taataagaag aataagaaga agagagatga ggtgggggag aagaagaaga 420 acaaatggtc atgcttcgat agctgttgtt ggtgggtggg gtgcatttgc acattgtggt 480 gttttcttct gtttctgtat cagatgatgc cttcttcgat tcctcagtat gtgaccgagg 540 ccttcactgg gcccatgccg gacccaccgg gcctcaaact caagaaggaa ggactcaagg 600 tgaagcaccc tgtggttttt gtgcccggga ttgtcactgg ggggcttgaa ctgtgggagg 660 gtcacctgtg tgctgagggg ttgttcagga aacgcttatg gggtggtacc ttcggagaag 720 tttataaaag accttcatgc tgggtggatc acatgtcact ggacaatgaa acaggattgg 780 atccaccagg gataagagtt aggcctgtct ctggacttgt agctgctgat tactttgctg 840 caggatactt tgtatgggca gtgctaattg ctaacttggc acgcattggt tatgaagaaa 900 aaactatgta catggctgca tatgattgga gaatagcatt tcagaacact gaggtgaggg 960 atcaaacact aagtcggata aaaagcaaca tagaacttat ggttgctact aatggtggaa 1020 ataaggcagt tattattcca cattcaatgg gggtcttgta ctttcttcat tttatgaagt 1080 gggttgaagc accagctcca actggtggtg gaggaggacc agattggtgc tccacatata 1140 taaaggcagt tgtaaacatt ggtggaccat ttttaggtgt tcccaaggct atagcagggc 1200 ttttctcagc tgaggcccgg gatattgctg ttgctaggac aatagctcca ggatttttag 1260 ataacgatct gtttcgcatt caaacattgc aacatgtaat gaagatgacc cgtacttggg 1320 actcaacaat gtcaatgata ccaagaggag gagatactat atggggtggt cttgattggt 1380 caccagaaga aggctatcac cctagccaga gaaagcacag caataacaat actcagttga 1440 aagaccacga aacaaatcaa acaaattttg tcaactatgg aagaatgata tcatttggca 1500 gagatgtggc cgaggcacac tcccctgaga ttcagatgac tgacttccgg ggtgctatca 1560 agggtcgcag tattgcaaat accacttgtc gtgatgtgtg gactgaatac catgaaatgg 1620 gatttgaagg agtgagagca gttgctgaac ataaagttta cacagctggc tcagtcgttg 1680 acctccttca atttgttgct ccaaagatga tggctcgtgg tagtgctcat ttctcttatg 1740 gaattgctga caatttggat gaccctaaat ataatcacta caagtattgg tcaaacccct 1800 tggaaacaaa attaccaaat gctcctgata tggaaatctt ctctatgtat ggagttggct 1860 tacctactga aagatcttat atttacaagt taactccctt tgccgagtgt tacattcctt 1920 ttgaaattga caccacacaa gatggtggta gcgatgaaga tagctgtctg caaggtggag 1980 tctacactgt tgatggggat gagactgtgc cggttctaag ttcaggcttc atgtgtgcta 2040 aaggttggcg cggaaaaaca agattcaacc catccggtat ccgcacctac gttagagaat 2100 atgatcattc tcctccagcc aaccttctag agggaagggg cacacaaagt ggtgctcacg 2160 ttgacatcat gggaaatttt gcattgattg aggatgttat aagagtggct gctggagcca 2220 aaggagaaga tctaggaggt gataaagtgt attctgatat cttcaagtgg tctgagaaaa 2280 tcaagttacc cctatgaatg aagcccaatg cacttccaca gttccactca gacacttctc 2340 ttgaacccct ttaaggatca gatcaggcta tatataattt ttgcagtata ttttcactgc 2400 caccagagtt ctgtaagttg cacttattag aattgctggt tctgctgatc aaattccagt 2460 tccatggagg ggtgaactat gcgaattggt tatattgtaa gagcttgtat tgaacatttt 2520 tgttattaaa gtaaggattt gatttgtcat ctctgagcaa cctggccagg ggcattattc 2580 ttaataagtt cagctggtta gttacgaaaa aaaaaaaaaa aaaataggtg tggattttat 2640 gtcagaaaat gtgcgtgcca tccttgatca agctggtttc agtgaggttg gcgtgtatag 2700 gatgtcaaat gagcaaattg gatgttctct ggctgatgcg gcagctactc gtacttacat 2760 ggaatatctt acagctgctt ctaggtctac ttctttgcat gtcatataca ttaacactaa 2820 gttagagaca aaggcatatg ctcatgaact tgtgcctaca ataacctgta cttcatcaaa 2880 tgttgtccag actatcctac aggcatttgc tcaagttcca gatttgagca tattttatgg 2940 acctgattct tacatgggtg caaatatcaa agatttgttc caacaaatga caaaaatgac 3000 tgatgaagag attgctgcaa tacatcctga gcacagtcaa gactctatta gatcattact 3060 acctcgactt cactattttc aggatggaac gtgcattgtt caccatctat ttggccatga 3120 ggttgtggag aagataaaag aaatgtactg tgatgcattc cttactgccc atcttgaggt 3180 acctggagag atgttttcat tggcaatgga agcaaagaga aggggaatgg gtgtagtagg 3240 ctccacaaag aatattttgg atttcataaa ggacagggtt caggaagctt tggatagaaa 3300 tatagatgat catctccaat ttgttttagg aacagaatct gggatggtga cttcaattgt 3360 ggcaacagtt cgtagtttgt tggagcctgt gaagtcctct tctgaaagag caaaagttac 3420 tgttgaaata gtctttccag tttcatcaga ctcaatctca acgaccacct caagtttatc 3480 ctccggcctt cagactgcca aagtgggtga tatcatactt cctgttgtac caggaatagc 3540 tagcggggag ggctgttcaa ttcatggtgg ctgtgcatct tgtccataca tgaagatgaa 3600 ttctcttggc tcactcctga aagttagcaa tcacctaccc gatgaagaaa atatcctttc 3660 tgcatacaag gcagagcgat ttaagttgca aacaccgaat ggcagatcag tggcagatgt 3720 tggatgtgaa cctattttgc acatgaggaa cttccaggct actaaaaagc ttccagagaa 3780 gcttgttgat cagattcttc gtccccaaca cagttgaagg ttgatgtgat aaagttgaga 3840 aataatgtgg tgatgtgaag aagacagaaa tttgtggtgc tgtcttgtga gcaattccaa 3900 gtagcaacta cagcaaaagt taggtccgtg caagggcttt gcttatagca tggtaatagt 3960 tgatacaacc agatttgttg tatgatagtt tcccttcgca taggggactt ctaatttatt 4020 tagataagat gacattatag agttcgatat caatatagag aaataaatga actagaaaaa 4080 aaaaaaaaaa aaa 4093 36 676 PRT Glycine max 36 Met Ser Leu Leu Arg Arg Arg Lys Gly Ser Glu Pro Glu Lys Gly Pro 1 5 10 15 Ser Pro Ser Ser Glu Pro Lys Val Leu Ser Glu Asp Glu Thr Glu Asp 20 25 30 Asp Lys Asn Asn Lys Lys Asn Lys Lys Lys Arg Asp Glu Val Gly Glu 35 40 45 Lys Lys Lys Asn Lys Trp Ser Cys Phe Asp Ser Cys Cys Trp Trp Val 50 55 60 Gly Cys Ile Cys Thr Leu Trp Cys Phe Leu Leu Phe Leu Tyr Gln Met 65 70 75 80 Met Pro Ser Ser Ile Pro Gln Tyr Val Thr Glu Ala Phe Thr Gly Pro 85 90 95 Met Pro Asp Pro Pro Gly Leu Lys Leu Lys Lys Glu Gly Leu Lys Val 100 105 110 Lys His Pro Val Val Phe Val Pro Gly Ile Val Thr Gly Gly Leu Glu 115 120 125 Leu Trp Glu Gly His Leu Cys Ala Glu Gly Leu Phe Arg Lys Arg Leu 130 135 140 Trp Gly Gly Thr Phe Gly Glu Val Tyr Lys Arg Pro Ser Cys Trp Val 145 150 155 160 Asp His Met Ser Leu Asp Asn Glu Thr Gly Leu Asp Pro Pro Gly Ile 165 170 175 Arg Val Arg Pro Val Ser Gly Leu Val Ala Ala Asp Tyr Phe Ala Ala 180 185 190 Gly Tyr Phe Val Trp Ala Val Leu Ile Ala Asn Leu Ala Arg Ile Gly 195 200 205 Tyr Glu Glu Lys Thr Met Tyr Met Ala Ala Tyr Asp Trp Arg Ile Ala 210 215 220 Phe Gln Asn Thr Glu Val Arg Asp Gln Thr Leu Ser Arg Ile Lys Ser 225 230 235 240 Asn Ile Glu Leu Met Val Ala Thr Asn Gly Gly Asn Lys Ala Val Ile 245 250 255 Ile Pro His Ser Met Gly Val Leu Tyr Phe Leu His Phe Met Lys Trp 260 265 270 Val Glu Ala Pro Ala Pro Thr Gly Gly Gly Gly Gly Pro Asp Trp Cys 275 280 285 Ser Thr Tyr Ile Lys Ala Val Val Asn Ile Gly Gly Pro Phe Leu Gly 290 295 300 Val Pro Lys Ala Ile Ala Gly Leu Phe Ser Ala Glu Ala Arg Asp Ile 305 310 315 320 Ala Val Ala Arg Thr Ile Ala Pro Gly Phe Leu Asp Asn Asp Leu Phe 325 330 335 Arg Ile Gln Thr Leu Gln His Val Met Lys Met Thr Arg Thr Trp Asp 340 345 350 Ser Thr Met Ser Met Ile Pro Arg Gly Gly Asp Thr Ile Trp Gly Gly 355 360 365 Leu Asp Trp Ser Pro Glu Glu Gly Tyr His Pro Ser Gln Arg Lys His 370 375 380 Ser Asn Asn Asn Thr Gln Leu Lys Asp His Glu Thr Asn Gln Thr Asn 385 390 395 400 Phe Val Asn Tyr Gly Arg Met Ile Ser Phe Gly Arg Asp Val Ala Glu 405 410 415 Ala His Ser Pro Glu Ile Gln Met Thr Asp Phe Arg Gly Ala Ile Lys 420 425 430 Gly Arg Ser Ile Ala Asn Thr Thr Cys Arg Asp Val Trp Thr Glu Tyr 435 440 445 His Glu Met Gly Phe Glu Gly Val Arg Ala Val Ala Glu His Lys Val 450 455 460 Tyr Thr Ala Gly Ser Val Val Asp Leu Leu Gln Phe Val Ala Pro Lys 465 470 475 480 Met Met Ala Arg Gly Ser Ala His Phe Ser Tyr Gly Ile Ala Asp Asn 485 490 495 Leu Asp Asp Pro Lys Tyr Asn His Tyr Lys Tyr Trp Ser Asn Pro Leu 500 505 510 Glu Thr Lys Leu Pro Asn Ala Pro Asp Met Glu Ile Phe Ser Met Tyr 515 520 525 Gly Val Gly Leu Pro Thr Glu Arg Ser Tyr Ile Tyr Lys Leu Thr Pro 530 535 540 Phe Ala Glu Cys Tyr Ile Pro Phe Glu Ile Asp Thr Thr Gln Asp Gly 545 550 555 560 Gly Ser Asp Glu Asp Ser Cys Leu Gln Gly Gly Val Tyr Thr Val Asp 565 570 575 Gly Asp Glu Thr Val Pro Val Leu Ser Ser Gly Phe Met Cys Ala Lys 580 585 590 Gly Trp Arg Gly Lys Thr Arg Phe Asn Pro Ser Gly Ile Arg Thr Tyr 595 600 605 Val Arg Glu Tyr Asp His Ser Pro Pro Ala Asn Leu Leu Glu Gly Arg 610 615 620 Gly Thr Gln Ser Gly Ala His Val Asp Ile Met Gly Asn Phe Ala Leu 625 630 635 640 Ile Glu Asp Val Ile Arg Val Ala Ala Gly Ala Lys Gly Glu Asp Leu 645 650 655 Gly Gly Asp Lys Val Tyr Ser Asp Ile Phe Lys Trp Ser Glu Lys Ile 660 665 670 Lys Leu Pro Leu 675 

What is claimed is:
 1. An isolated polynucleotide comprising: (a) a nucleotide sequence encoding a polypeptide having phospholipid:diacylglycerol acyltransferase activity, wherein the polypeptide has an amino acid sequence of at least 80% sequence identity, based on the Clustal V method of alignment, when compared to one of SEQ ID NO:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 32, 34 or 36, or (b) a complement of the nucleotide sequence, wherein the complement and the nucleotide sequence consist of the same number of nucleotides and are 100% complementary.
 2. The polynucleotide of claim 1, wherein the amino acid sequence of the polypeptide has at least 85% sequence identity, based on the Clustal V method of alignment, when compared to one of SEQ ID NO:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 32, 34 or
 36. 3. The polynucleotide of claim 1, wherein the amino acid sequence of the polypeptide has at least 90% sequence identity, based on the Clustal V method of alignment, when compared to one of SEQ ID NO:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 32, 34 or
 36. 4. The polynucleotide of claim 1, wherein the amino acid sequence of the polypeptide has at least 95% sequence identity, based on the Clustal V method of alignment, when compared to one of SEQ ID NO:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 32, 34 or
 36. 5. The polynucleotide of claim 1, wherein the amino acid sequence of the polypeptide comprises one of SEQ ID NO:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 32, 34 or
 36. 6. The polynucleotide of claim 1 wherein the nucleotide sequence comprises one of SEQ ID NO:1, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 27, 31, 33 or
 35. 7. A vector comprising the polynucleotide of claim
 1. 8. A recombinant DNA construct comprising the polynucleotide of claim 1 operably linked to at least one regulatory sequence.
 9. A method for transforming a cell, comprising transforming a cell with the polynucleotide of claim
 1. 10. A cell comprising the recombinant DNA construct of claim
 8. 11. A method for producing a plant comprising transforming a plant cell with the polynucleotide of claim 1 and regenerating a plant from the transformed plant cell.
 12. A plant comprising the recombinant DNA construct of claim
 8. 13. A seed comprising the recombinant DNA construct of claim
 8. 14. An isolated polypeptide having phospholipid:diacylglycerol acyltransferase activity, wherein the polypeptide has an amino acid sequence of at least 80% sequence identity, based on the Clustal V method of alignment, when compared to one of SEQ ID NO:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 32, 34 or
 36. 15. The polypeptide of claim 14, wherein the amino acid sequence of the polypeptide has at least 85% sequence identity, based on the Clustal V method of alignment, when compared to one of SEQ ID NO:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 32, 34 or
 36. 16. The polypeptide of claim 14, wherein the amino acid sequence of the polypeptide has at least 90% sequence identity, based on the Clustal V method of alignment, when compared to one of SEQ ID NO:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 32, 34 or
 36. 17. The polypeptide of claim 14, wherein the amino acid sequence of the polypeptide has at least 95% sequence identity, based on the Clustal V method of alignment, when compared to one of SEQ ID NO:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 32, 34 or
 36. 18. The polypeptide of claim 14, wherein the amino acid sequence of the polypeptide comprises one of SEQ ID NO:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 32, 34 or
 36. 19. A method for isolating a polypeptide having phospholipid:diacylglycerol acyltransferase activity comprising isolating the polypeptide from a cell or culture medium of the cell, wherein the cell comprises a recombinant DNA construct comprising the polynucleotide of claim 1 operably linked to at least one regulatory sequence.
 20. A method of altering the level of expression of a phospholipid:diacylglycerol acyltransferase in a host cell comprising: (a) transforming a host cell with the recombinant DNA construct of claim 8; and (b) growing the transformed host cell under conditions that are suitable for expression of the recombinant DNA construct wherein expression of the recombinant DNA construct results in production of altered levels of the phospholipid:diacylglycerol acyltransferase in the transformed host cell. 